A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590906



Internal ID16378315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85490666..85576904hg38UCSC Ensembl
Innerchr3:85539816..85626054hg19UCSC Ensembl
Innerchr3:85622506..85708744hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3886239
hg1986239
hg1886239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967548
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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