A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398946



Internal ID21056499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29755515..29979004hg38UCSC Ensembl
chr6:29723292..29946781hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38223490
hg19223490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6107n223
Supporting Variantsnssv18221789
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)nsv6398946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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