A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526132



Internal ID15106739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2865294..2928727hg38UCSC Ensembl
Innerchr7:2904928..2968361hg19UCSC Ensembl
Innerchr7:2871454..2934887hg18UCSC Ensembl
Innerchr7:2678169..2741602hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3863434
hg1963434
hg1863434
hg1763434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702386
Samples
Known GenesCARD11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526132
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