A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339800



Internal ID20997353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207800221..207802349hg38UCSC Ensembl
chr2:208664945..208667073hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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