A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698785



Internal ID15435437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10803968..10807857hg38UCSC Ensembl
Innerchr17:10707285..10711174hg19UCSC Ensembl
Innerchr17:10648010..10651899hg18UCSC Ensembl
Innerchr17:10648010..10651899hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg383890
hg193890
hg183890
hg173890
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523093
Supporting Variants
Samples
Known GenesLINC00675, TMEM220-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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