A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656178



Internal ID15392830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62715937..62944328hg38UCSC Ensembl
Innerchr7:62176315..62404706hg19UCSC Ensembl
Innerchr7:61813750..62042141hg18UCSC Ensembl
Innerchr7:61620465..61848856hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38228392
hg19228392
hg18228392
hg17228392
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656178
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