A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866236



Internal ID16160192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949152..949686hg38UCSC Ensembl
Innerchr17:852392..852926hg19UCSC Ensembl
Innerchr17:799142..799676hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38535
hg19535
hg18535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574135
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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