A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427583



Internal ID21085136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84482101..84483000hg38UCSC Ensembl
chr8:85394336..85395235hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171952
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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