A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668231



Internal ID15058197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152772068..152802887hg38UCSC Ensembl
Innerchr4:153693220..153724039hg19UCSC Ensembl
Innerchr4:153912670..153943489hg18UCSC Ensembl
Innerchr4:154050825..154081644hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3830820
hg1930820
hg1830820
hg1730820
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516652
Supporting Variants
Samples
Known GenesARFIP1, TIGD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668231
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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