A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464846



Internal ID22522734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46582133..46585932hg38UCSC Ensembl
chr14:47051336..47055135hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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