A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630093



Internal ID21822140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:220822..220904hg38UCSC Ensembl
chr17:70613..70695hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037889
Supporting Variants
Samples
Known GenesRPH3AL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630093
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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