A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138723



Internal ID20705763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126173353..126176262hg38UCSC Ensembl
chr6:126494499..126497408hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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