A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549905



Internal ID16337314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5878873..5888616hg38UCSC Ensembl
Innerchr10:5920836..5930579hg19UCSC Ensembl
Innerchr10:5960842..5970585hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg389744
hg199744
hg189744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743523
Samples
Known GenesANKRD16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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