A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374565



Internal ID22600234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864633..106770579hg38UCSC Ensembl
chr14:106330843..107178821hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38905947
hg19847979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938492
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374565
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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