A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344826



Internal ID21002379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216748104..216748866hg38UCSC Ensembl
chr2:217612827..217613589hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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