A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864755



Internal ID22639690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5292727..5293897hg38UCSC Ensembl
chr10:5334690..5335860hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv146n209
Supporting Variantsnssv17453570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864755
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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