A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641340



Internal ID21833387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5122227..5123298hg38UCSC Ensembl
chr21:45558637..45559708hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052354
Supporting Variants
Samples
Known GenesC21orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641340
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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