A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590897



Internal ID16378306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85073473..85137935hg38UCSC Ensembl
Innerchr3:85122624..85187085hg19UCSC Ensembl
Innerchr3:85205314..85269775hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3864463
hg1964462
hg1864462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967539
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590897
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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