A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726887



Internal ID150553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39406997..39425906hg38UCSC Ensembl
chr21:40778923..40797832hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3818910
hg1918910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563276
Supporting Variants
Samples
Known GenesLCA5L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726887
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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