A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389258



Internal ID22447128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88607433..88608258hg38UCSC Ensembl
chr14:89073777..89074602hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936245
Supporting Variants
Samples
Known GenesZC3H14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389258
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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