A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841157



Internal ID22616092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141096445..141103681hg38UCSC Ensembl
chr5:140476029..140483265hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg387237
hg197237
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495603
Samples
Known GenesPCDHB2, PCDHB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841157
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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