A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862155



Internal ID22637090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103313064..103317639hg38UCSC Ensembl
chr14:103779401..103783976hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384576
hg194576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862155
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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