A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880164



Internal ID22655134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52699..64895hg38UCSC Ensembl
chr18:52699..64895hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3812197
hg1912197
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478574, nssv17471346, nssv17478575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880164
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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