A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013531



Internal ID18756062
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 StatusM
Merged Variants
Supporting Variantsnssv3593971, nssv3593970
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)nsv1013531
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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