A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134707



Internal ID20701747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105468344..105468661hg38UCSC Ensembl
chr6:105916219..105916536hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00145


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