A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684792



Internal ID15074758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133492654..133524462hg38UCSC Ensembl
Innerchr10:135306158..135337966hg19UCSC Ensembl
Innerchr10:135156148..135187956hg18UCSC Ensembl
Innerchr10:135195039..135226847hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3831809
hg1931809
hg1831809
hg1731809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684792
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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