A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002453



Internal ID19091670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60405824..60661807hg38UCSC Ensembl
Innerchr3:60391557..60647540hg19UCSC Ensembl
Innerchr3:60366597..60622580hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38255984
hg19255984
hg18255984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4753n100
Supporting Variantsnssv3593418
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)nsv1002453
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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