A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388540



Internal ID22446410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50487829..50495887hg38UCSC Ensembl
chr17:48565190..48573248hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg388059
hg198059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388540
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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