A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860085



Internal ID22635020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32992896..32997395hg38UCSC Ensembl
chr14:33462102..33466601hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463303
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860085
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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