A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011133



Internal ID19100350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60323811..60431606hg38UCSC Ensembl
Innerchr3:60309541..60417339hg19UCSC Ensembl
Innerchr3:60284581..60392379hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38107796
hg19107799
hg18107799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4751n100
Supporting Variantsnssv3593410
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)nsv1011133
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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