A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372597



Internal ID22598266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863395..106556923hg38UCSC Ensembl
chr14:106329605..107012923hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38693529
hg19683319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944737
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372597
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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