A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454698



Internal ID22512574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38718496..38729809hg38UCSC Ensembl
chr14:39187700..39199013hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3811314
hg1911314
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454698
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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