A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921499



Internal ID22696723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36510005..36549087hg38UCSC Ensembl
chr10:36798933..36838015hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3839083
hg1939083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921499
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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