A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129276



Internal ID20696316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180407101..180421100hg38UCSC Ensembl
chr5:179834101..179848100hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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