A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733861



Internal ID157527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9048300..9056604hg38UCSC Ensembl
chr21:9887133..9895437hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg388305
hg198305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009863


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