A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570804



Internal ID16011527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100878753..100880008hg38UCSC Ensembl
Innerchr15:101418958..101420213hg19UCSC Ensembl
Innerchr15:99236481..99237736hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381256
hg191256
hg181256
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv850953, nssv850952
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570804
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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