A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654732



Internal ID15044698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150959613..150962138hg38UCSC Ensembl
Innerchr4:151880765..151883290hg19UCSC Ensembl
Innerchr4:152100215..152102740hg18UCSC Ensembl
Innerchr4:152238370..152240895hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382526
hg192526
hg182526
hg172526
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517186
Supporting Variants
Samples
Known GenesLRBA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654732
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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