A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861340



Internal ID22636275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120848381..120850145hg38UCSC Ensembl
chr10:122607893..122609657hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466075
Samples
Known GenesMIR5694, WDR11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861340
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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