A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213302



Internal ID20780342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151869001..151875700hg38UCSC Ensembl
chr5:151248562..151255261hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411609
Supporting Variants
Samples
Known GenesGLRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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