A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353263



Internal ID21010816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:198716901..198718500hg38UCSC Ensembl
chr2:199581625..199583224hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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