A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843576



Internal ID15790846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58260407..58560264hg38UCSC Ensembl
Innerchr15:58552606..58852463hg19UCSC Ensembl
Innerchr15:56339898..56639755hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38299858
hg19299858
hg18299858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569598
Supporting Variants
Samples
Known GenesLIPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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