A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595689



Internal ID16036412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150867803..151094552hg38UCSC Ensembl
Innerchr4:151788955..152015704hg19UCSC Ensembl
Innerchr4:152008405..152235154hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38226750
hg19226750
hg18226750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009403
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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