A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673596



Internal ID15410248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114768535..114797087hg38UCSC Ensembl
Innerchr10:116528294..116556846hg19UCSC Ensembl
Innerchr10:116518284..116546836hg18UCSC Ensembl
Innerchr10:116518284..116546836hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3828553
hg1928553
hg1828553
hg1728553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516803
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673596
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