A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612397



Internal ID16399806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136833690hg38UCSC Ensembl
Innerchr8:137687955..137845933hg19UCSC Ensembl
Innerchr8:137757137..137915115hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38157979
hg19157979
hg18157979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156172, nssv1122266, nssv1156171
Samples1798860594_A, 1780862002_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612397
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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