A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482589



Internal ID22540494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14248078..14291581hg38UCSC Ensembl
chr20:14228724..14272227hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843504
hg1943504
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870550
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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