A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358379



Internal ID22584048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306315..114306368hg38UCSC Ensembl
chr10:116066074..116066127hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917791
Supporting Variants
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358379
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03


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