A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875605



Internal ID16169561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58130370..58141352hg38UCSC Ensembl
Innerchr17:56207731..56218713hg19UCSC Ensembl
Innerchr17:53562730..53573712hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810983
hg1910983
hg1810983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575778
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)nssv875605
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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