A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570222



Internal ID16357631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79505903..79512970hg38UCSC Ensembl
Innerchr15:79798245..79805312hg19UCSC Ensembl
Innerchr15:77585300..77592367hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387068
hg197068
hg187068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847502, nssv847503
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570222
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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