A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590411



Internal ID16377820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61136645..61142459hg38UCSC Ensembl
Innerchr3:61122318..61128132hg19UCSC Ensembl
Innerchr3:61097358..61103172hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385815
hg195815
hg185815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963414
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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