A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418310



Internal ID21075863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117525108..117525544hg38UCSC Ensembl
chr8:118537347..118537783hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163781
Samples
Known GenesMED30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418310
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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