A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637871



Internal ID21829918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36054834..36054902hg38UCSC Ensembl
chr21:37427132..37427200hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051876
Supporting Variants
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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