A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570288



Internal ID16011011
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 StatusM
Merged Variantsdgv4690n54
Supporting Variantsnssv1149252
SamplesHGDP00562
Known GenesALPK3, SLC28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570288
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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