A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546197



Internal ID18497792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46088437..46164298hg38UCSC Ensembl
Innerchr17:44165803..44241664hg19UCSC Ensembl
Innerchr17:41521621..41597441hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3875862
hg1975862
hg1875821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059880
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)nssv3546197
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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