A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740220



Internal ID15687490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1327073..1327546hg38UCSC Ensembl
Innerchr10:1369268..1369741hg19UCSC Ensembl
Innerchr10:1359268..1359741hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38474
hg19474
hg18474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549789
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)nssv740220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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