A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612705



Internal ID21804752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34857141..34857252hg38UCSC Ensembl
chr14:35326347..35326458hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026097
Supporting Variants
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612705
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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