A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733877



Internal ID157543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9734222..9737279hg38UCSC Ensembl
chr4_gl000193_random:1536..4593hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733877
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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