A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017672



Internal ID22079303
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155998
Supporting Variants
Samples
Known GenesCADM2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017672
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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