A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516803



Internal ID15444096
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674966, nssv671040, nssv662133, nssv673596
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516803
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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