A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465701



Internal ID22523590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102571948..102573247hg38UCSC Ensembl
chr14:103038285..103039584hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465701
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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