A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137142



Internal ID20704182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116300375..116302520hg38UCSC Ensembl
chr6:116621538..116623683hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg382146
hg192146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606150
Supporting Variants
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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