A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141896



Internal ID20708936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14983833..14986225hg38UCSC Ensembl
chr6:14984064..14986456hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382393
hg192393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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