A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008386



Internal ID19097604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82662952..82719539hg38UCSC Ensembl
Innerchr3:82712103..82768690hg19UCSC Ensembl
Innerchr3:82794793..82851380hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3856588
hg1956588
hg1856588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4800n100
Supporting Variantsnssv3596242
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)nsv1008386
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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