A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427371



Internal ID21084924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140194801..140196300hg38UCSC Ensembl
chr8:141204900..141206399hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167231
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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