A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867043



Internal ID22641978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11111961..11115060hg38UCSC Ensembl
chr10:11153924..11157023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468692
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867043
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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