A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382188



Internal ID22440058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64527244..64528118hg38UCSC Ensembl
chr14:64993962..64994836hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946581
Supporting Variants
Samples
Known GenesZBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382188
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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