A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867629



Internal ID22642564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50235511..50238022hg38UCSC Ensembl
chr18:47761881..47764392hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg382512
hg192512
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478546
Samples
Known GenesCCDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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