A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850925



Internal ID22625860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74103228..74110877hg38UCSC Ensembl
chr14:74569931..74577580hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387650
hg197650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461815
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850925
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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