A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340329



Internal ID20997882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:49866938..49907504hg38UCSC Ensembl
chr2:50094076..50134642hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3840567
hg1940567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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