A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129280



Internal ID20696320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180420067..180430265hg38UCSC Ensembl
chr5:179847067..179857265hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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