A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614572



Internal ID16055295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69504046hg38UCSC Ensembl
Innerchr9:72100051..72118962hg19UCSC Ensembl
Innerchr9:71289871..71308782hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818912
hg1918912
hg1818912
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137111, nssv1137115, nssv1176074, nssv1176070, nssv1176081, nssv1176079, nssv1176073, nssv1176083, nssv1176075, nssv1176076, nssv1137110, nssv1137113, nssv1176082, nssv1137105, nssv1137108, nssv1176077, nssv1137107, nssv1137109, nssv1176078, nssv1137114, nssv1176071, nssv1137116, nssv1137112, nssv1176072, nssv1137106, nssv1176069, nssv1176080
SamplesHGDP00203, HGDP01294, 1780862043_A, HGDP00125, HGDP01343, HGDP00167, 1780862345_A, HGDP00688, HGDP00557, HGDP01088, HGDP00571, HGDP00727, HGDP00454, HGDP00460, HGDP00579
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614572
Frequency
Sample Size17421
Observed Gain4
Observed Loss23
Observed Complex0
Frequencyn/a


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