A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215598



Internal ID20782638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134060185..134064700hg38UCSC Ensembl
chr6:134381323..134385838hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg384516
hg194516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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