A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414681



Internal ID21072234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29884698..29923181hg38UCSC Ensembl
chr6:29852475..29890958hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3838484
hg1938484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6116n223
Supporting Variantsnssv18141398
Samples
Known GenesHLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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