A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699288



Internal ID15435940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45685097..45696087hg38UCSC Ensembl
Innerchr7:45724696..45735686hg19UCSC Ensembl
Innerchr7:45691221..45702211hg18UCSC Ensembl
Innerchr7:45497936..45508926hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3810991
hg1910991
hg1810991
hg1710991
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523515
Supporting Variants
Samples
Known GenesADCY1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer