A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866431



Internal ID16160387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2052523..2059100hg38UCSC Ensembl
Innerchr17:1955817..1962394hg19UCSC Ensembl
Innerchr17:1902567..1909144hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg386578
hg196578
hg186578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574220
Supporting Variants
Samples
Known GenesHIC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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