A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353585



Internal ID21011138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199688161..199688979hg38UCSC Ensembl
chr2:200552884..200553702hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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