A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612371



Internal ID16399780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136670241..136829820hg38UCSC Ensembl
Innerchr8:137682484..137842063hg19UCSC Ensembl
Innerchr8:137751666..137911245hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38159580
hg19159580
hg18159580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122205
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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