A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743522



Internal ID15690792
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 StatusS
Merged Variantsnsv549904
Supporting Variants
Samples
Known GenesANKRD16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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