A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421464



Internal ID21079017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73356146..73361242hg38UCSC Ensembl
chr8:74268381..74273477hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385097
hg195097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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