A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454538



Internal ID22512414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71411374..71418152hg38UCSC Ensembl
chr14:71878091..71884869hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg386779
hg196779
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454538
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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