A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350789



Internal ID21008342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159234195..159242478hg38UCSC Ensembl
chr2:160090706..160098989hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg388284
hg198284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079908
Samples
Known GenesWDSUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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