A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127475



Internal ID20694515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159973867..159974196hg38UCSC Ensembl
chr5:159400874..159401203hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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