A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854560



Internal ID22629495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91363246..91366422hg38UCSC Ensembl
chr10:93123003..93126179hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383177
hg193177
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456527
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854560
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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