A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570805



Internal ID16358214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100878753..100880220hg38UCSC Ensembl
Innerchr15:101418958..101420425hg19UCSC Ensembl
Innerchr15:99236481..99237948hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381468
hg191468
hg181468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4781n54
Supporting Variantsnssv850955, nssv850954
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570805
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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