A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619809



Internal ID20992880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119641629..119698044hg38UCSC Ensembl
chr6:119962790..120019201hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3856416
hg1956412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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