A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871390



Internal ID22646328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61625838..61676023hg38UCSC Ensembl
chr20:60200894..60251079hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3850186
hg1950186
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486775
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871390
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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