A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430024



Internal ID21087577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34807801..34824100hg38UCSC Ensembl
chr8:34665319..34681618hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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