A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865896



Internal ID22640831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57199619..57212642hg38UCSC Ensembl
chr10:58959379..58972402hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3813024
hg1913024
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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