A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865133



Internal ID22640068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11640517..11651617hg38UCSC Ensembl
chr10:11682516..11693616hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3811101
hg1911101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865133
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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