A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236021



Internal ID20803061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73840101..73936100hg38UCSC Ensembl
chr6:74549798..74645816hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3896000
hg1996019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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