A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615439



Internal ID21807486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88607927..88607981hg38UCSC Ensembl
chr14:89074271..89074325hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033334
Supporting Variants
Samples
Known GenesZC3H14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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