A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591242



Internal ID16031965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105654992..105751290hg38UCSC Ensembl
Innerchr3:105373836..105470134hg19UCSC Ensembl
Innerchr3:106856526..106952824hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3896299
hg1996299
hg1896299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971265
Samples
Known GenesCBLB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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