A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660010



Internal ID15049976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86961278..86973435hg38UCSC Ensembl
Innerchr10:88721035..88733192hg19UCSC Ensembl
Innerchr10:88711015..88723172hg18UCSC Ensembl
Innerchr10:88711015..88723172hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3812158
hg1912158
hg1812158
hg1712158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517487
Supporting Variants
Samples
Known GenesADIRF, AGAP11, SNCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660010
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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