A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519708



Internal ID18471303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49720681..49811144hg38UCSC Ensembl
Innerchr10:50928727..51019190hg19UCSC Ensembl
Innerchr10:50598733..50689196hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3890464
hg1990464
hg1890464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048905
Supporting Variants
Samples
Known GenesOGDHL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519708
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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