A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524424



Internal ID15451717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105544971..105570354hg38UCSC Ensembl
Innerchr4:106466128..106491511hg19UCSC Ensembl
Innerchr4:106685577..106710960hg18UCSC Ensembl
Innerchr4:106823732..106849115hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3825384
hg1925384
hg1825384
hg1725384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700350
Samples
Known GenesARHGEF38, ARHGEF38-IT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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