A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590910



Internal ID16378319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85604283..85645837hg38UCSC Ensembl
Innerchr3:85653433..85694987hg19UCSC Ensembl
Innerchr3:85736123..85777677hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3841555
hg1941555
hg1841555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8424n54
Supporting Variantsnssv1152492
SamplesHGDP01213
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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