A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837642



Internal ID22612577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120759982..120817445hg38UCSC Ensembl
chr4:121681137..121738600hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3857464
hg1957464
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490159
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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