A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724184



Internal ID18675779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46147167..46214780hg38UCSC Ensembl
Innerchr17:44224533..44292146hg19UCSC Ensembl
Innerchr17:41580310..41647923hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3867614
hg1967614
hg1867614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061617
Supporting Variants
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724184
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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