A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151870



Internal ID15507610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10477996..10486091hg38UCSC Ensembl
Innerchr3:10519680..10527775hg19UCSC Ensembl
Innerchr3:10494680..10502775hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388096
hg198096
hg188096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589654
Supporting Variants
Samples1780862075_A
Known GenesATP2B2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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