A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831526



Internal ID22606461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138894469..138900616hg38UCSC Ensembl
chr2:139652039..139658186hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg386148
hg196148
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487684
Samples
Known GenesYY1P2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831526
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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