A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590410



Internal ID16377819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61054612..61068673hg38UCSC Ensembl
Innerchr3:61040284..61054345hg19UCSC Ensembl
Innerchr3:61015324..61029385hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3814062
hg1914062
hg1814062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151902
Samples1780862085_A
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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