A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612134



Internal ID16399543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121991818..122048281hg38UCSC Ensembl
Innerchr8:123004057..123060520hg19UCSC Ensembl
Innerchr8:123073238..123129701hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3856464
hg1956464
hg1856464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156869
Samples1780862195_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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