A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432574



Internal ID21090127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135981602..135982193hg38UCSC Ensembl
chr8:136993845..136994436hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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