A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400895



Internal ID21058448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89338965..89341026hg38UCSC Ensembl
chr6:90048684..90050745hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382062
hg192062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148098
Samples
Known GenesUBE2J1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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