A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006588



Internal ID19095805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:78432819..78448370hg38UCSC Ensembl
Innerchr3:78481969..78497520hg19UCSC Ensembl
Innerchr3:78564659..78580210hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3815552
hg1915552
hg1815552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596223, nssv3596224
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)nsv1006588
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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