A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000732



Internal ID19089949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21935477..21970749hg38UCSC Ensembl
Innerchr3:21976969..22012241hg19UCSC Ensembl
Innerchr3:21951973..21987245hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3835273
hg1935273
hg1835273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4694n100
Supporting Variantsnssv3593165
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)nsv1000732
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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