A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589717



Internal ID16030440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12898047..12935363hg38UCSC Ensembl
Innerchr3:12939546..12976863hg19UCSC Ensembl
Innerchr3:12914546..12951863hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3837317
hg1937318
hg1837318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959129
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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