A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387372



Internal ID22445242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105891713..106511112hg38UCSC Ensembl
chr14:106357571..106967044hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38619400
hg19609474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935737
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387372
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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