A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215145



Internal ID20782185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180663008..180679067hg38UCSC Ensembl
chr5:180090008..180106067hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3816060
hg1916060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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