A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861461



Internal ID22636396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49301354..49304053hg38UCSC Ensembl
chr8:50213913..50216612hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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