A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629461



Internal ID21821508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45883339..45883406hg38UCSC Ensembl
chr17:43960705..43960772hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028980
Supporting Variants
Samples
Known GenesMAPT-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629461
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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