A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035526



Internal ID19124745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14895994..15022388hg38UCSC Ensembl
Innerchr16:14989851..15116245hg19UCSC Ensembl
Innerchr16:14897352..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38126395
hg19126395
hg18126395
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2752n100
Supporting Variantsnssv3557639, nssv3718934, nssv3557660, nssv3718936, nssv3557653, nssv3718933, nssv3557671, nssv3557675, nssv3557641, nssv3557647, nssv3557652, nssv3557662, nssv3557648, nssv3557656, nssv3557658, nssv3557654, nssv3557674, nssv3557669, nssv3557661, nssv3557657, nssv3557650, nssv3557670, nssv3557646, nssv3557640, nssv3557673, nssv3557666, nssv3557644, nssv3557663, nssv3718942, nssv3718941, nssv3557676, nssv3557672, nssv3718935, nssv3557642, nssv3718940, nssv3718939, nssv3557664, nssv3718937, nssv3557668, nssv3557659, nssv3557645, nssv3557655, nssv3557649, nssv3557651, nssv3718938, nssv3557638, nssv3557667, nssv3557665, nssv3718943, nssv3557643
Samples
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035526
Frequency
Sample Size11257
Observed Gain2
Observed Loss48
Observed Complex0
Frequencyn/a


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