A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593391



Internal ID18544986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58504269..60217021hg38UCSC Ensembl
Innerchr3:58489996..60202749hg19UCSC Ensembl
Innerchr3:58465036..60177789hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381712753
hg191712754
hg181712754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012688
Supporting Variants
Samples
Known GenesACOX2, C3orf67, FAM107A, FAM3D, FHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593391
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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