A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999478



Internal ID19159015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21930369..21970749hg38UCSC Ensembl
Innerchr3:21971861..22012241hg19UCSC Ensembl
Innerchr3:21946865..21987245hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3840381
hg1940381
hg1840381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4694n100
Supporting Variantsnssv3593162
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)nsv999478
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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