A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836614



Internal ID22611549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52596184..52597608hg38UCSC Ensembl
chr3:52630200..52631624hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1457n209
Supporting Variantsnssv17493240, nssv17493239
Samples
Known GenesPBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836614
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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