A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578738



Internal ID16366147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17150608..17150908hg38UCSC Ensembl
Innerchr19:17261418..17261718hg19UCSC Ensembl
Innerchr19:17122418..17122718hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38301
hg19301
hg18301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6292n54
Supporting Variantsnssv895699, nssv895629, nssv895653, nssv895637, nssv895722, nssv895729, nssv895607, nssv895673, nssv895668, nssv895688, nssv895669, nssv895596, nssv895593, nssv895616, nssv895681, nssv895685, nssv895652, nssv895650, nssv895708, nssv895648, nssv895715, nssv895679, nssv895713, nssv895600, nssv895672, nssv895665, nssv895658, nssv895622, nssv895712, nssv895687, nssv895632, nssv895718, nssv895612, nssv895618, nssv895726, nssv895674, nssv895716, nssv895649, nssv895602, nssv895714, nssv895617, nssv895683, nssv895621, nssv895700, nssv895625, nssv895628, nssv895642, nssv895698, nssv895663, nssv895630, nssv895624, nssv895710, nssv895610, nssv895633, nssv895627, nssv895667, nssv895641, nssv895719, nssv895720, nssv895704, nssv895702, nssv895707, nssv895608, nssv895657, nssv895638, nssv895651, nssv895635, nssv895643, nssv895689, nssv895697, nssv895601, nssv895686, nssv895675, nssv895626, nssv895639, nssv895678, nssv895646, nssv895692, nssv895613, nssv895684, nssv895634, nssv895680, nssv895705, nssv895599, nssv895615, nssv895661, nssv895660, nssv895609, nssv895701, nssv895670, nssv895724, nssv895723, nssv895706, nssv895725, nssv895691, nssv895605, nssv895676, nssv895728, nssv895614, nssv895711, nssv895659, nssv895640, nssv895671, nssv895664, nssv895631, nssv895644, nssv895620, nssv895703, nssv895730, nssv895682, nssv895721, nssv895655, nssv895619, nssv895654, nssv895656, nssv895645, nssv895603, nssv895695, nssv895709, nssv895636, nssv895594, nssv895696, nssv895727, nssv895595, nssv895606, nssv895690, nssv895677, nssv895694, nssv895647, nssv895611, nssv895592, nssv895717, nssv895623, nssv895598, nssv895666, nssv895597, nssv895604, nssv895693, nssv895662
Samples
Known GenesMYO9B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578738
Frequency
Sample Size17421
Observed Gain0
Observed Loss139
Observed Complex0
Frequencyn/a


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