A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006443



Internal ID18748974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36361829..36476267hg38UCSC Ensembl
Innerchr3:36403321..36517759hg19UCSC Ensembl
Innerchr3:36378325..36492763hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38114439
hg19114439
hg18114439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589659
Samples
Known GenesSTAC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006443
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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