A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128020



Internal ID20695060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149691082..149696634hg38UCSC Ensembl
chr5:149070645..149076197hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385553
hg195553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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