A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv867000



Internal ID16160956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13924402..13942124hg38UCSC Ensembl
Innerchr17:13827719..13845441hg19UCSC Ensembl
Innerchr17:13768444..13786166hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3817723
hg1917723
hg1817723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574387
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)nssv867000
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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