A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123882



Internal ID20690923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12342258..12506714hg38UCSC Ensembl
chr5:12342370..12506826hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38164457
hg19164457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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