A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344582



Internal ID21002135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25052790..25077484hg38UCSC Ensembl
chr2:25275659..25300353hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3824695
hg1924695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085577
Samples
Known GenesEFR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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