A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337325



Internal ID20994878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23963253..24089139hg38UCSC Ensembl
chr2:24186123..24312009hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38125887
hg19125887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208389
Samples
Known GenesC2orf44, FKBP1B, MFSD2B, SF3B14, TP53I3, UBXN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337325
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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