A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834169



Internal ID22609104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99736634..99739633hg38UCSC Ensembl
chr2:100353096..100356095hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489129
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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