A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570361



Internal ID16357770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87248887..87320484hg38UCSC Ensembl
Innerchr15:87792118..87863715hg19UCSC Ensembl
Innerchr15:85593122..85664719hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3871598
hg1971598
hg1871598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4702n54
Supporting Variantsnssv848135
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570361
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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