A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138348



Internal ID20705388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137607040..137619001hg38UCSC Ensembl
chr6:137928177..137940138hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3811962
hg1911962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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