A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv867187



Internal ID16161143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14286645..14294134hg38UCSC Ensembl
Innerchr17:14189962..14197451hg19UCSC Ensembl
Innerchr17:14130687..14138176hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg387490
hg197490
hg187490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574395
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)nssv867187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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