A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383035



Internal ID22440905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50413450..50417435hg38UCSC Ensembl
chr17:48490811..48494796hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg383986
hg193986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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