A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213184



Internal ID20780224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126744720..126773188hg38UCSC Ensembl
chr5:126080412..126108880hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3828469
hg1928469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213184
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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