A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583571



Internal ID16024294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165158204..165159681hg38UCSC Ensembl
Innerchr2:166014714..166016191hg19UCSC Ensembl
Innerchr2:165722960..165724437hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381478
hg191478
hg181478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7155n54
Supporting Variantsnssv925187
Samples
Known GenesSCN3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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