A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865785



Internal ID22640720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25669409..25670487hg38UCSC Ensembl
chr10:25958338..25959416hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455115
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865785
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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