A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574122



Internal ID16361531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948992..949808hg38UCSC Ensembl
Innerchr17:852232..853048hg19UCSC Ensembl
Innerchr17:798982..799798hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38817
hg19817
hg18817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5399n54
Supporting Variantsnssv866125
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574122
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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