A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832097



Internal ID22607032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1892408..1897679hg38UCSC Ensembl
chr2:1896180..1901451hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg385272
hg195272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488807
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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