A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468541



Internal ID22526430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66634149..66651638hg38UCSC Ensembl
chr14:67100867..67118356hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3817490
hg1917490
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862055
Supporting Variants
Samples
Known GenesGPHN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468541
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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