A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570383



Internal ID16357792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87480491..87518591hg38UCSC Ensembl
Innerchr15:88023722..88061822hg19UCSC Ensembl
Innerchr15:85824726..85862826hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3838101
hg1938101
hg1838101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848197
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570383
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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