A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595691



Internal ID16036414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150929372..150962138hg38UCSC Ensembl
Innerchr4:151850524..151883290hg19UCSC Ensembl
Innerchr4:152069974..152102740hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3832767
hg1932767
hg1832767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009405, nssv1009406
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595691
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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