A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611423



Internal ID16398832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60945654..60957090hg38UCSC Ensembl
Innerchr8:61858213..61869649hg19UCSC Ensembl
Innerchr8:62020767..62032203hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3811437
hg1911437
hg1811437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12181n54
Supporting Variantsnssv1115645, nssv1156843, nssv1115643, nssv1115646, nssv1156844, nssv1115642, nssv1115641, nssv1115647, nssv1115644
SamplesHGDP01378, HGDP01079
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611423
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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