A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862888



Internal ID22637823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23572769..23577518hg38UCSC Ensembl
chr10:23861698..23866447hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384750
hg194750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463444, nssv17452721, nssv17459431, nssv17455344, nssv17451003, nssv17453120, nssv17460938, nssv17455027, nssv17467588, nssv17465223, nssv17461638, nssv17459079, nssv17455291, nssv17467472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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