A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138983



Internal ID20706023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139279401..139287000hg38UCSC Ensembl
chr6:139600538..139608137hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619732
Supporting Variants
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02327


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