A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003387



Internal ID19092605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59770638..59845614hg38UCSC Ensembl
Innerchr3:59756364..59831340hg19UCSC Ensembl
Innerchr3:59731404..59806380hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3874977
hg1974977
hg1874977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731127
Samples
Known GenesFHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003387
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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