A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727032



Internal ID150698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42024536..42027184hg38UCSC Ensembl
chr21:43444645..43447293hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535480
Supporting Variants
Samples
Known GenesZNF295-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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