A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383678



Internal ID22441548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863247..106511115hg38UCSC Ensembl
chr14:106329457..106967047hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38647869
hg19637591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937068
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383678
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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