A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620950



Internal ID21812997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45969567..45969669hg38UCSC Ensembl
chr17:44046933..44047035hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036820
Supporting Variants
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620950
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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