A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429054



Internal ID21086607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37973803..37974925hg38UCSC Ensembl
chr8:37831321..37832443hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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