A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137332



Internal ID20704372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122052751..122053079hg38UCSC Ensembl
chr6:122373897..122374225hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004


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