A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889558



Internal ID22664577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32652283..32751588hg38UCSC Ensembl
chr6:32620060..32719365hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3899306
hg1999306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429787
Samples
Known GenesHLA-DQA2, HLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889558
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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