A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612394



Internal ID16399803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675295..136851516hg38UCSC Ensembl
Innerchr8:137687538..137863759hg19UCSC Ensembl
Innerchr8:137756720..137932941hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38176222
hg19176222
hg18176222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156168, nssv1156169
SamplesHGDP00892, HGDP00155
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612394
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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