A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396925



Internal ID21054478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29804733..29959858hg38UCSC Ensembl
chr6:29772510..29927635hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38155126
hg19155126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6109n223
Supporting Variantsnssv18141384
Samples
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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