A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674132



Internal ID15410784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111588117..111638389hg38UCSC Ensembl
Innerchr7:111228173..111278445hg19UCSC Ensembl
Innerchr7:111015409..111065681hg18UCSC Ensembl
Innerchr7:110822124..110872396hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3850273
hg1950273
hg1850273
hg1750273
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674132
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