A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617996



Internal ID21810043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44568290..44569055hg38UCSC Ensembl
chr17:42645658..42646423hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617996
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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