A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869623



Internal ID15816893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32486261..32486852hg38UCSC Ensembl
Innerchr17:30813279..30813870hg19UCSC Ensembl
Innerchr17:27837392..27837983hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38592
hg19592
hg18592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574703
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)nssv869623
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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