A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614995



Internal ID21807042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21793608..21831269hg38UCSC Ensembl
chr14:22261779..22299425hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3837662
hg1937647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614995
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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