A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855477



Internal ID15802747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28823218..28824174hg38UCSC Ensembl
Innerchr16:28834539..28835495hg19UCSC Ensembl
Innerchr16:28742040..28742996hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38957
hg19957
hg18957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571804
Supporting Variants
Samples
Known GenesATXN2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855477
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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