A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592026



Internal ID16379435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149551336..149552236hg38UCSC Ensembl
Innerchr3:149269123..149270023hg19UCSC Ensembl
Innerchr3:150751813..150752713hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8648n54
Supporting Variantsnssv976676, nssv976673, nssv976661, nssv976650, nssv976664, nssv976684, nssv976638, nssv976687, nssv976675, nssv976646, nssv976674, nssv976663, nssv976681, nssv976691, nssv976654, nssv976694, nssv976672, nssv976686, nssv976685, nssv976660, nssv976640, nssv976682, nssv976637, nssv976669, nssv976651, nssv976658, nssv976649, nssv976693, nssv976680, nssv976667, nssv976695, nssv976656, nssv976688, nssv976639, nssv976643, nssv976668, nssv976652, nssv976683, nssv976671, nssv976690, nssv976642, nssv976655, nssv976648, nssv976641, nssv976689, nssv976662, nssv976670, nssv976678, nssv976666, nssv976644, nssv976645, nssv976696, nssv976657, nssv976698, nssv976697, nssv976692, nssv976653, nssv976659, nssv976677, nssv976679, nssv976647, nssv976665
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592026
Frequency
Sample Size17421
Observed Gain0
Observed Loss62
Observed Complex0
Frequencyn/a


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