A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337779



Internal ID20995332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23942583..23946620hg38UCSC Ensembl
chr2:24165453..24169490hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384038
hg194038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084488
Samples
Known GenesUBXN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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