A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848188



Internal ID16142144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87287299..87338866hg38UCSC Ensembl
Innerchr15:87830530..87882097hg19UCSC Ensembl
Innerchr15:85631534..85683101hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3851568
hg1951568
hg1851568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570375
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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