A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877549



Internal ID22652514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61518371..61521834hg38UCSC Ensembl
chr18:59185604..59189067hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471396
Samples
Known GenesCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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