A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137040



Internal ID20704080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109213934..109220561hg38UCSC Ensembl
chr6:109535137..109541764hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386628
hg196628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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