A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570223



Internal ID16357632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79510521..79512970hg38UCSC Ensembl
Innerchr15:79802863..79805312hg19UCSC Ensembl
Innerchr15:77589918..77592367hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382450
hg192450
hg182450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4678n54
Supporting Variantsnssv847504, nssv847505
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570223
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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