A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862186



Internal ID22637121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23871554..23877111hg38UCSC Ensembl
chr10:24160483..24166040hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385558
hg195558
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469426
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862186
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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