A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575099



Internal ID21523524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161571558..161653408hg38UCSC Ensembl
chr1:161541348..161623198hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881851
hg1981851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061036
SamplesHG03732
Known GenesFCGR2C, FCGR3B, HSPA7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575099
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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