A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549366



Internal ID16336775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234066399..234119277hg38UCSC Ensembl
Innerchr1:234202145..234255023hg19UCSC Ensembl
Innerchr1:232268768..232321646hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3852879
hg1952879
hg1852879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv857n54
Supporting Variantsnssv738114
Samples
Known GenesSLC35F3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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