A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148859



Internal ID15874429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38754598..38789516hg38UCSC Ensembl
Innerchr15:39046799..39081717hg19UCSC Ensembl
Innerchr15:36834091..36869009hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3834919
hg1934919
hg1834919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569205
Supporting Variants
SamplesHGDP00540
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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