A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463855



Internal ID22521741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23090949..23098682hg38UCSC Ensembl
chr14:23560158..23567891hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387734
hg197734
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861793
Supporting Variants
Samples
Known GenesACIN1, C14orf119
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463855
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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