A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351099



Internal ID21008652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136322230..136337703hg38UCSC Ensembl
chr2:137079800..137095273hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3815474
hg1915474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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