A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549964



Internal ID15990687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10785719..10963741hg38UCSC Ensembl
Innerchr10:10827682..11005704hg19UCSC Ensembl
Innerchr10:10867688..11045710hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38178023
hg19178023
hg18178023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744006
Samples
Known GenesLINC00710, SFTA1P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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