A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374253



Internal ID22599922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13874122..13878253hg38UCSC Ensembl
chr17:13777439..13781570hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384132
hg194132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374253
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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