A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703638



Internal ID15440290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46198867..46235741hg38UCSC Ensembl
Innerchr8:47110489..47147363hg19UCSC Ensembl
Innerchr8:47229654..47266528hg18UCSC Ensembl
Innerchr8:47229654..47266528hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3836875
hg1936875
hg1836875
hg1736875
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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