A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872379



Internal ID15819649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46092442..46215654hg38UCSC Ensembl
Innerchr17:44169808..44293020hg19UCSC Ensembl
Innerchr17:41525626..41648797hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38123213
hg19123213
hg18123172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575163
Supporting Variants
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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