A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374695



Internal ID21032248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86062154..86062622hg38UCSC Ensembl
chr3:86111304..86111772hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106071
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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