A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832304



Internal ID22607239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1866217..1868790hg38UCSC Ensembl
chr2:1869989..1872562hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg382574
hg192574
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488791
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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