A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703569



Internal ID15093535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134952791..135157183hg38UCSC Ensembl
Innerchr7:134637542..134841935hg19UCSC Ensembl
Innerchr7:134288082..134492475hg18UCSC Ensembl
Innerchr7:134094797..134299190hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38204393
hg19204394
hg18204394
hg17204394
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527174
Supporting Variants
Samples
Known GenesAGBL3, CALD1, TMEM140
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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