A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958578



Internal ID22733640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64214212..64214307hg38UCSC Ensembl
chr20:62845565..62845660hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404606
Samples
Known GenesMYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958578
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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