A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549776



Internal ID15990499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237571..1240333hg38UCSC Ensembl
Innerchr10:1281487..1282372hg19UCSC Ensembl
Innerchr10:1271487..1272372hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382763
hg19886
hg18886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv927n54
Supporting Variantsnssv740185, nssv740186, nssv740184, nssv740188, nssv740187
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549776
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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