A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850052



Internal ID22624987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15391886..15432938hg38UCSC Ensembl
chr10:15433885..15474937hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3841053
hg1941053
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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