A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406261



Internal ID21063814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29768774..29913854hg38UCSC Ensembl
chr6:29736551..29881631hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38145081
hg19145081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230884
Samples
Known GenesHCG4, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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