A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574957



Internal ID16015680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37803179..37850528hg38UCSC Ensembl
Innerchr17:36163150..36210152hg19UCSC Ensembl
Innerchr17:33237263..33284265hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3847350
hg1947003
hg1847003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870490
Samples
Known GenesYWHAEP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574957
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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