A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637938



Internal ID21829985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16577404..16577492hg38UCSC Ensembl
chr21:17949724..17949812hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042194
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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