A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574598



Internal ID16015321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20911453..20969018hg38UCSC Ensembl
Innerchr17:20814766..20872331hg19UCSC Ensembl
Innerchr17:20755358..20812923hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3857566
hg1957566
hg1857566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5502n54
Supporting Variantsnssv1149758
SamplesHGDP00099
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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