A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847800



Internal ID22622735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45864479..45872475hg38UCSC Ensembl
chr10:46359927..46367923hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387997
hg197997
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n209
Supporting Variantsnssv17449942, nssv17469309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847800
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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