A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634201



Internal ID21826248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65630303..65632005hg38UCSC Ensembl
chr17:63626421..63628123hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381703
hg191703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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