A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893304



Internal ID22668363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29833095..30011611hg38UCSC Ensembl
chr6:29800872..29979388hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38178517
hg19178517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446367
Samples
Known GenesHCG4B, HCG9, HLA-A, HLA-H, HLA-J, ZNRD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893304
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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