A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416181



Internal ID21073734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102550732..102551117hg38UCSC Ensembl
chr8:103562960..103563345hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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