A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683093



Internal ID15419745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149786285..149802324hg38UCSC Ensembl
Innerchr7:149483373..149499412hg19UCSC Ensembl
Innerchr7:149114306..149130345hg18UCSC Ensembl
Innerchr7:148921021..148937060hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3816040
hg1916040
hg1816040
hg1716040
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517242
Supporting Variants
Samples
Known GenesSSPO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683093
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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