A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575803



Internal ID16016526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59222156..59245593hg38UCSC Ensembl
Innerchr17:57299517..57322954hg19UCSC Ensembl
Innerchr17:54654299..54677736hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3823438
hg1923438
hg1823438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875647
Samples
Known GenesGDPD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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