A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146495



Internal ID20713535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78610980..78611317hg38UCSC Ensembl
chr6:79320697..79321034hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395979
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0017


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