A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612377



Internal ID16399786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136670241..136843055hg38UCSC Ensembl
Innerchr8:137682484..137855298hg19UCSC Ensembl
Innerchr8:137751666..137924480hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38172815
hg19172815
hg18172815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122215
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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