A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887380



Internal ID22662372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37103892..37107212hg38UCSC Ensembl
chr20:35732295..35735615hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383321
hg193321
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485384, nssv17485385
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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