A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702453



Internal ID15439105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35673742..35830884hg38UCSC Ensembl
Innerchr3:35715234..35872376hg19UCSC Ensembl
Innerchr3:35690238..35847380hg18UCSC Ensembl
Innerchr3:35690238..35847380hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38157143
hg19157143
hg18157143
hg17157143
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526191
Supporting Variants
Samples
Known GenesARPP21, MIR128-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702453
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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