A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545162



Internal ID18496757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46078703..46138096hg38UCSC Ensembl
Innerchr17:44156069..44215462hg19UCSC Ensembl
Innerchr17:41511888..41571239hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3859394
hg1959394
hg1859352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061156
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)nssv3545162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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