A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001320



Internal ID19090537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68402059..68425978hg38UCSC Ensembl
Innerchr3:68451209..68475128hg19UCSC Ensembl
Innerchr3:68533899..68557818hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3823920
hg1923920
hg1823920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4770n100
Supporting Variantsnssv3593975
Samples
Known GenesFAM19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001320
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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