A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866456



Internal ID15813726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3601921..3664167hg38UCSC Ensembl
Innerchr17:3505215..3567461hg19UCSC Ensembl
Innerchr17:3451964..3514210hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3862247
hg1962247
hg1862247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574241
Supporting Variants
Samples
Known GenesCTNS, P2RX5-TAX1BP3, SHPK, TAX1BP3, TRPV1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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