A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351942



Internal ID21009495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73934604..73943327hg38UCSC Ensembl
chr2:74161731..74170454hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg388724
hg198724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090365
Samples
Known GenesDGUOK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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