A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974400



Internal ID50303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135946807..135957251hg38UCSC Ensembl
chr5:135282496..135292940hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3810445
hg1910445
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558422
Supporting Variants
Samples
Known GenesLECT2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974400
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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