A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705879



Internal ID15095845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152748252..152903963hg38UCSC Ensembl
Innerchr4:153669404..153825115hg19UCSC Ensembl
Innerchr4:153888854..154044565hg18UCSC Ensembl
Innerchr4:154027009..154182720hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38155712
hg19155712
hg18155712
hg17155712
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522511
Supporting Variants
Samples
Known GenesARFIP1, TIGD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705879
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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