A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487342



Internal ID22545258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64209313..64211847hg38UCSC Ensembl
chr20:62840666..62843200hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871498
Supporting Variants
Samples
Known GenesMYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487342
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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