A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549967



Internal ID16337376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11936500..12031470hg38UCSC Ensembl
Innerchr10:11978499..12073469hg19UCSC Ensembl
Innerchr10:12018505..12113475hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3894971
hg1994971
hg1894971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv955n54
Supporting Variantsnssv744009
Samples
Known GenesUPF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549967
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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