A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590300



Internal ID16377709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52056581..52062416hg38UCSC Ensembl
Innerchr3:52090597..52096432hg19UCSC Ensembl
Innerchr3:52065637..52071472hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg385836
hg195836
hg185836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963088
Samples
Known GenesLINC00696
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590300
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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