A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837913



Internal ID22612848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133149633..133152168hg38UCSC Ensembl
chr4:134070788..134073323hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382536
hg192536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492865
Samples
Known GenesPCDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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