A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455273



Internal ID22513150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61363702..61372998hg38UCSC Ensembl
chr14:61830420..61839716hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg389297
hg199297
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857651
Supporting Variants
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455273
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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