A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864829



Internal ID22639764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23412156..23416307hg38UCSC Ensembl
chr10:23701085..23705236hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384152
hg194152
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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