A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391359



Internal ID22449229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16593728..16596318hg38UCSC Ensembl
chr21:17966048..17968638hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957306
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391359
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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