A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551627



Internal ID16339036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79801605..79903819hg38UCSC Ensembl
Innerchr10:81561361..81663575hg19UCSC Ensembl
Innerchr10:81520800..81653555hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38102215
hg19102215
hg18132756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751841
Samples
Known GenesLOC642361
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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