A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423319



Internal ID21080872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73799826..73801550hg38UCSC Ensembl
chr8:74712061..74713785hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381725
hg191725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169451
Samples
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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