A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884348



Internal ID22659330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10813986..10842217hg38UCSC Ensembl
chr18:10813984..10842215hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3828232
hg1928232
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477114
Samples
Known GenesPIEZO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884348
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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