A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418589



Internal ID21076142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61350282..61350868hg38UCSC Ensembl
chr8:62262841..62263427hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168723
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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