A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740169



Internal ID15687439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1120460..1308893hg38UCSC Ensembl
Innerchr10:1166400..1351088hg19UCSC Ensembl
Innerchr10:1156400..1341088hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38188434
hg19184689
hg18184689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549768
Supporting Variants
Samples
Known GenesADARB2, LINC00200, WDR37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv740169
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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