A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853622



Internal ID22628557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75054227..75058841hg38UCSC Ensembl
chr14:75520930..75525544hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455612
Samples
Known GenesACYP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853622
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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