A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493598



Internal ID19081239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..130672hg38UCSC Ensembl
Innerchr10:72797..176612hg19UCSC Ensembl
Innerchr10:62797..166612hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38103812
hg19103816
hg18103816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050312
Supporting Variants
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493598
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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