A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343341



Internal ID21000894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161082307..161098710hg38UCSC Ensembl
chr2:161938818..161955221hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3816404
hg1916404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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