A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416098



Internal ID21073651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57971455..57977142hg38UCSC Ensembl
chr8:58884014..58889701hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385688
hg195688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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