A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461830



Internal ID22519715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65088821..65090617hg38UCSC Ensembl
chr14:65555539..65557335hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381797
hg191797
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850138
Supporting Variants
Samples
Known GenesLOC100506321, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461830
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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