A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407273



Internal ID21064826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29765941..29995995hg38UCSC Ensembl
chr6:29733718..29963772hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38230055
hg19230055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6108n223
Supporting Variantsnssv18141375
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)nsv6407273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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