A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873924



Internal ID22648874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7679346..7682078hg38UCSC Ensembl
chr18:7679344..7682076hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472100
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873924
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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