A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416662



Internal ID21074215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21053741..21059072hg38UCSC Ensembl
chr8:20911252..20916583hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385332
hg195332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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