A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127069



Internal ID20694109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153007193..153013067hg38UCSC Ensembl
chr5:152386753..152392627hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg385875
hg195875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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