A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570363



Internal ID16357772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87256693..87319578hg38UCSC Ensembl
Innerchr15:87799924..87862809hg19UCSC Ensembl
Innerchr15:85600928..85663813hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3862886
hg1962886
hg1862886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4702n54
Supporting Variantsnssv848137, nssv1149260
SamplesNINDS_260
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570363
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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