A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150603



Internal ID20717643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97831618..97832143hg38UCSC Ensembl
chr6:98279494..98280019hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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