A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406579



Internal ID21064132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32995249..33154154hg38UCSC Ensembl
chr6:32963026..33121931hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38158906
hg19158906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142243
Samples
Known GenesHLA-DOA, HLA-DPA1, HLA-DPB1, HLA-DPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406579
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