A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605966



Internal ID20979037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127352025..127354502hg38UCSC Ensembl
chr6:127673170..127675647hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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