A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654765



Internal ID15391417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149781233..149803904hg38UCSC Ensembl
Innerchr7:149478321..149500992hg19UCSC Ensembl
Innerchr7:149109254..149131925hg18UCSC Ensembl
Innerchr7:148915969..148938640hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3822672
hg1922672
hg1822672
hg1722672
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)nssv654765
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