A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425488



Internal ID21083041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142845352..142851762hg38UCSC Ensembl
chr8:143926768..143933178hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386411
hg196411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167379
Samples
Known GenesGML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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