A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590074



Internal ID16377483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37936223..37944834hg38UCSC Ensembl
Innerchr3:37977714..37986325hg19UCSC Ensembl
Innerchr3:37952718..37961329hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg388612
hg198612
hg188612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8282n54
Supporting Variantsnssv962159, nssv962161, nssv962163, nssv962162, nssv962160
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590074
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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