A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872769



Internal ID15820039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46379862..46487204hg38UCSC Ensembl
Innerchr17:44457228..44564570hg19UCSC Ensembl
Innerchr17:41812971..41919886hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38107343
hg19107343
hg18106916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575354
Supporting Variants
Samples
Known GenesNSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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