A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568917



Internal ID16009640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32874970..33011971hg38UCSC Ensembl
Innerchr15:33167171..33304172hg19UCSC Ensembl
Innerchr15:30954463..31091464hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38137002
hg19137002
hg18137002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839795
Samples
Known GenesFMN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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