A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871498



Internal ID22646436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64209313..64211847hg38UCSC Ensembl
chr20:62840666..62843200hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487342
Samples
Known GenesMYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871498
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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