A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419516



Internal ID21077069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59291233..59291629hg38UCSC Ensembl
chr8:60203792..60204188hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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