A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148872



Internal ID15853712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53788613..53864783hg38UCSC Ensembl
Innerchr15:54080810..54156980hg19UCSC Ensembl
Innerchr15:51868102..51944272hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3876171
hg1976171
hg1876171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569452
Supporting Variants
Samples1780854382_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148872
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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