A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375577



Internal ID22601246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864350..106627257hg38UCSC Ensembl
chr14:106330560..107083262hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38762908
hg19752703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935698
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375577
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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