A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870550



Internal ID22645486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14248078..14291581hg38UCSC Ensembl
chr20:14228724..14272227hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843504
hg1943504
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482590, nssv17482589
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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