A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380579



Internal ID22438449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58488483..58488735hg38UCSC Ensembl
chr17:56565844..56566096hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380579
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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