A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867710



Internal ID22642645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61679861..61701715hg38UCSC Ensembl
chr20:60254917..60276771hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3821855
hg1921855
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486780
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867710
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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