A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455612



Internal ID22513489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75054227..75058841hg38UCSC Ensembl
chr14:75520930..75525544hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853622
Supporting Variants
Samples
Known GenesACYP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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