A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491773



Internal ID18732728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1149274..1244688hg38UCSC Ensembl
Innerchr10:1195214..1286740hg19UCSC Ensembl
Innerchr10:1185214..1276740hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3895415
hg1991527
hg1891527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041995
Supporting Variants
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3491773
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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