A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149252



Internal ID15527928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84872155..84919085hg38UCSC Ensembl
Innerchr15:85415386..85462316hg19UCSC Ensembl
Innerchr15:83216390..83263320hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3846931
hg1946931
hg1846931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570288
Supporting Variants
SamplesHGDP00562
Known GenesALPK3, SLC28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149252
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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