A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527113



Internal ID15107720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150393163..150395282hg38UCSC Ensembl
Innerchr4:151314315..151316434hg19UCSC Ensembl
Innerchr4:151533765..151535884hg18UCSC Ensembl
Innerchr4:151671920..151674039hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382120
hg192120
hg182120
hg172120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703495
Samples
Known GenesLRBA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527113
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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