A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155998



Internal ID22086503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85589241..85724431hg38UCSC Ensembl
Outerchr3:85581008..85727065hg38UCSC Ensembl
Innerchr3:85638391..85773581hg19UCSC Ensembl
Outerchr3:85630158..85776215hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38146058
hg19146058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017672
Samples
Known GenesCADM2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155998
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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