A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417842



Internal ID21075395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59797320..59797832hg38UCSC Ensembl
chr8:60709879..60710391hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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