A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850592



Internal ID22625527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88489866..88529125hg38UCSC Ensembl
chr14:88956210..88995469hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3839260
hg1939260
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469727
Samples
Known GenesPTPN21
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850592
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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