A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151896



Internal ID15878449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59835345..59942001hg38UCSC Ensembl
Innerchr3:59821071..59927727hg19UCSC Ensembl
Innerchr3:59796111..59902767hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38106657
hg19106657
hg18106657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590384
Supporting Variants
SamplesHGDP01203
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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