A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382706



Internal ID22440576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21540074..21543404hg38UCSC Ensembl
chr14:22008208..22011550hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383331
hg193343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382706
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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