A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702276



Internal ID15092242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127345104..127358156hg38UCSC Ensembl
Innerchr7:126985158..126998210hg19UCSC Ensembl
Innerchr7:126772394..126785446hg18UCSC Ensembl
Innerchr7:126579109..126592161hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3813053
hg1913053
hg1813053
hg1713053
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526043
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702276
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