A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343939



Internal ID21001492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84456612..84458271hg38UCSC Ensembl
chr2:84683736..84685395hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381660
hg191660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092208
Samples
Known GenesSUCLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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