A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569601



Internal ID16357010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58508567..58573957hg38UCSC Ensembl
Innerchr15:58800766..58866156hg19UCSC Ensembl
Innerchr15:56588058..56653448hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865391
hg1965391
hg1865391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843579
Samples
Known GenesLIPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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