A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509208



Internal ID18460803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83270389..84629720hg38UCSC Ensembl
Innerchr10:85030145..86389476hg19UCSC Ensembl
Innerchr10:85020125..86379456hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381359332
hg191359332
hg181359332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046749
Supporting Variants
Samples
Known GenesC10orf99, CCSER2, CDHR1, GHITM, LINC00858, LRIT1, LRIT2, RGR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509208
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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