A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699016



Internal ID15435668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51789821..51793622hg38UCSC Ensembl
Innerchr18:49316191..49319992hg19UCSC Ensembl
Innerchr18:47570189..47573990hg18UCSC Ensembl
Innerchr18:47570189..47573990hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg383802
hg193802
hg183802
hg173802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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