A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624762



Internal ID21816809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15979830..15979883hg38UCSC Ensembl
chr17:15883144..15883197hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031648
Supporting Variants
Samples
Known GenesZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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