A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375358



Internal ID21032911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123199989..123208341hg38UCSC Ensembl
chr3:122918836..122927188hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg388353
hg198353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095226
Samples
Known GenesSEC22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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