A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851643



Internal ID22626578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3827839..3831047hg38UCSC Ensembl
chr10:3870031..3873239hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383209
hg193209
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463740, nssv17468365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851643
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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