A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883141



Internal ID22658119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1965130..1965489hg38UCSC Ensembl
chr2:1968902..1969261hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398363
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883141
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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