A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552128



Internal ID20925258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39656874..39657610hg38UCSC Ensembl
chr21:41028801..41029537hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072417
Samples
Known GenesB3GALT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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