A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398877



Internal ID21056430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32638411..32742381hg38UCSC Ensembl
chr6:32606188..32710158hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38103971
hg19103971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6158n223
Supporting Variantsnssv18142212
Samples
Known GenesHLA-DQA1, HLA-DQA2, HLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer