A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868859



Internal ID15816129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17507716..17519294hg38UCSC Ensembl
Innerchr17:17411030..17422608hg19UCSC Ensembl
Innerchr17:17351755..17363333hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3811579
hg1911579
hg1811579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574525
Supporting Variants
Samples
Known GenesPEMT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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