A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704633



Internal ID15441285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110632371..110662639hg38UCSC Ensembl
Innerchr7:110272427..110302695hg19UCSC Ensembl
Innerchr7:110059663..110089931hg18UCSC Ensembl
Innerchr7:109866378..109896646hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3830269
hg1930269
hg1830269
hg1730269
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528095
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704633
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