A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628344



Internal ID21820391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18268457..18268512hg38UCSC Ensembl
chr17:18171771..18171826hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628344
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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