A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856979



Internal ID22631914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101731547..101745276hg38UCSC Ensembl
chr10:103491304..103505033hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3813730
hg1913730
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856979
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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