A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014601



Internal ID18757136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59680883..59902440hg38UCSC Ensembl
Innerchr3:59666609..59888166hg19UCSC Ensembl
Innerchr3:59641649..59863206hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38221558
hg19221558
hg18221558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593396
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)nsv1014601
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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