A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549904



Internal ID15990627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5851305..5874238hg38UCSC Ensembl
Innerchr10:5893268..5916201hg19UCSC Ensembl
Innerchr10:5933274..5956207hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3822934
hg1922934
hg1822934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743522
Samples
Known GenesANKRD16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549904
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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