A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556809



Internal ID18508404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46147167..46168761hg38UCSC Ensembl
Innerchr17:44224533..44246127hg19UCSC Ensembl
Innerchr17:41580310..41601904hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3821595
hg1921595
hg1821595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059256
Supporting Variants
Samples
Known GenesKANSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556809
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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