A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593970



Internal ID18545565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67867347..68020883hg38UCSC Ensembl
Innerchr3:67917771..68070027hg19UCSC Ensembl
Innerchr3:68000461..68152717hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38153537
hg19152257
hg18152257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013531
Supporting Variants
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)nssv3593970
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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