A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917791



Internal ID22693012
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 StatusM
Merged Variants
Supporting Variantsnssv17358379
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917791
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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