A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590911



Internal ID16378320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85739857..85771266hg38UCSC Ensembl
Innerchr3:85789007..85820416hg19UCSC Ensembl
Innerchr3:85871697..85903106hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3831410
hg1931410
hg1831410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152493
Samples1782681093_A
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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