A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132258



Internal ID20699298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74786108..74792342hg38UCSC Ensembl
chr5:74081933..74088167hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg386235
hg196235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414089
Supporting Variants
Samples
Known GenesFAM169A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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