A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694995



Internal ID15084961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6150149..6173025hg38UCSC Ensembl
Innerchr7:6189780..6212656hg19UCSC Ensembl
Innerchr7:6156306..6179181hg18UCSC Ensembl
Innerchr7:5963021..5985896hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3822877
hg1922877
hg1822876
hg1722876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522217
Supporting Variants
Samples
Known GenesCYTH3, USP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694995
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