A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133604



Internal ID20700644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52636652..52638667hg38UCSC Ensembl
chr5:51932486..51934501hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382016
hg192016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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