A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740183



Internal ID15687453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237571..1240317hg38UCSC Ensembl
Innerchr10:1281487..1282332hg19UCSC Ensembl
Innerchr10:1271487..1272332hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382747
hg19846
hg18846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549775
Supporting Variants
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv740183
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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