A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698079



Internal ID15434731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123160655..123165686hg38UCSC Ensembl
Innerchr8:124172895..124177926hg19UCSC Ensembl
Innerchr8:124242076..124247107hg18UCSC Ensembl
Innerchr8:124242076..124247107hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385032
hg195032
hg185032
hg175032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521469
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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