A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875820



Internal ID16169776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65088877..65115334hg38UCSC Ensembl
Innerchr17:63084995..63111452hg19UCSC Ensembl
Innerchr17:60515457..60541914hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3826458
hg1926458
hg1826458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575872
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875820
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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