A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849846



Internal ID22624781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101283182..101284974hg38UCSC Ensembl
chr10:103042939..103044731hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381793
hg191793
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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