A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004322



Internal ID19093539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26498302..26541717hg38UCSC Ensembl
Innerchr3:26539793..26583208hg19UCSC Ensembl
Innerchr3:26514797..26558212hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3843416
hg1943416
hg1843416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4711n100
Supporting Variantsnssv3589553
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)nsv1004322
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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