A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698944



Internal ID15088910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135080396..135111234hg38UCSC Ensembl
Innerchr7:134765148..134795986hg19UCSC Ensembl
Innerchr7:134415688..134446526hg18UCSC Ensembl
Innerchr7:134222403..134253241hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3830839
hg1930839
hg1830839
hg1730839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523222
Supporting Variants
Samples
Known GenesAGBL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698944
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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