A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217120



Internal ID20784160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15145426..15146140hg38UCSC Ensembl
chr6:15145657..15146371hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402876
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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