A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467509



Internal ID22525400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22962892..22965091hg38UCSC Ensembl
chr14:23432101..23434300hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850979
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467509
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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