A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408943



Internal ID21066496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55036112..55043755hg38UCSC Ensembl
chr6:54900910..54908553hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg387644
hg197644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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