A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842013



Internal ID22616948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:22278876..22284046hg38UCSC Ensembl
chr5:22278985..22284155hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg385171
hg195171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499099
Samples
Known GenesCDH12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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