A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009260



Internal ID19098478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80256224..80368161hg38UCSC Ensembl
Innerchr3:80305374..80417311hg19UCSC Ensembl
Innerchr3:80388064..80500001hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38111938
hg19111938
hg18111938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596230
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009260
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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