A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828072



Internal ID22603007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161669113..161675884hg38UCSC Ensembl
chr1:161638903..161645674hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg386772
hg196772
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465571
Samples
Known GenesFCGR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828072
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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