A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384622



Internal ID22442492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6057140..6059478hg38UCSC Ensembl
chr17:5960460..5962798hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg382339
hg192339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384622
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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