A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468765



Internal ID22526654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49880943..49891392hg38UCSC Ensembl
chr14:50347661..50358110hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3810450
hg1910450
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468765
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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