A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570504



Internal ID16357913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93134682..93444927hg38UCSC Ensembl
Innerchr15:93677911..93988156hg19UCSC Ensembl
Innerchr15:91478915..91789160hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38310246
hg19310246
hg18310246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848926
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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