A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359996



Internal ID21017549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86070401..86075200hg38UCSC Ensembl
chr3:86119551..86124350hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106073
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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