A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126804



Internal ID20693844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154174591..154178679hg38UCSC Ensembl
chr5:153554151..153558239hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384089
hg194089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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