A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851481



Internal ID22626416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130683312..130701354hg38UCSC Ensembl
chr10:132481576..132499618hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3818043
hg1918043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851481
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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