A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880984



Internal ID22655955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8280945..8283044hg38UCSC Ensembl
chr18:8280943..8283042hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472606, nssv17472605
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880984
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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