A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344780



Internal ID21002333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100508136..100510866hg38UCSC Ensembl
chr2:101124598..101127328hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382731
hg192731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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