A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344420



Internal ID21001973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204218701..204226900hg38UCSC Ensembl
chr2:205083424..205091623hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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