A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467264



Internal ID22525155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83144543..83151454hg38UCSC Ensembl
chr14:83610887..83617798hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg386912
hg196912
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467264
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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