A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866756



Internal ID15814026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8160445..8173097hg38UCSC Ensembl
Innerchr17:8063763..8076415hg19UCSC Ensembl
Innerchr17:8004488..8017140hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3812653
hg1912653
hg1812653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574336
Supporting Variants
Samples
Known GenesTMEM107, VAMP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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