A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346054



Internal ID21003607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84457669..84475855hg38UCSC Ensembl
chr2:84684793..84702979hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3818187
hg1918187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092209
Samples
Known GenesSUCLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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