A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213251



Internal ID20780291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145297101..145332500hg38UCSC Ensembl
chr5:144676664..144712063hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3835400
hg1935400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213251
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00258


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