A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674797



Internal ID15064763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90556437..90592034hg38UCSC Ensembl
Innerchr7:90185751..90221348hg19UCSC Ensembl
Innerchr7:90023687..90059284hg18UCSC Ensembl
Innerchr7:89830402..89865999hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835598
hg1935598
hg1835598
hg1735598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515998
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674797
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer