A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517536



Internal ID15098143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150277928..150278345hg38UCSC Ensembl
Innerchr4:151199080..151199497hg19UCSC Ensembl
Innerchr4:151418530..151418947hg18UCSC Ensembl
Innerchr4:151556685..151557102hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38418
hg19418
hg18418
hg17418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674005, nssv652291
Samples
Known GenesLRBA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517536
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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