A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833889



Internal ID22608824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98195733..98200243hg38UCSC Ensembl
chr2:98812196..98816706hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483074
Samples
Known GenesVWA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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