A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500416



Internal ID18741371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1133579..1495256hg38UCSC Ensembl
Innerchr10:1179519..1537451hg19UCSC Ensembl
Innerchr10:1169519..1527451hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38361678
hg19357933
hg18357933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045618
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)nssv3500416
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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