A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859813



Internal ID22634748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17828214..17832626hg38UCSC Ensembl
chr10:17870213..17874625hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384413
hg194413
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456007
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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