A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720639



Internal ID18672234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46120237..46177128hg38UCSC Ensembl
Innerchr17:44197603..44254494hg19UCSC Ensembl
Innerchr17:41553381..41610271hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3856892
hg1956892
hg1856891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055618
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)nssv3720639
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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