A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407281



Internal ID21064834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29769236..29999448hg38UCSC Ensembl
chr6:29737013..29967225hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38230213
hg19230213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6108n223
Supporting Variantsnssv18141377
Samples
Known GenesHCG4, HCG4B, HCG9, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407281
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