A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426239



Internal ID21083792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117520701..117521200hg38UCSC Ensembl
chr8:118532940..118533439hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163780
Samples
Known GenesMED30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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