A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858882



Internal ID22633817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96733042..96736236hg38UCSC Ensembl
chr10:98492799..98495993hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383195
hg193195
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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