A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352454



Internal ID22578123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11262940..11262940hg38UCSC Ensembl
chr10:11304903..11304903hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959278
Supporting Variants
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352454
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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