A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370266



Internal ID22595935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94950491..94956022hg38UCSC Ensembl
chr14:95416828..95422359hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385532
hg195532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370266
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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