A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606019



Internal ID21798066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23232820..23232896hg38UCSC Ensembl
chr14:23702029..23702105hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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