A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2n171



Internal ID22814364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114328109..114328579hg38UCSC Ensembl
chr10:116087868..116088338hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4389573, nsv4389562, nsv4389561
Samples
Known GenesAFAP1L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)dgv2n171
Frequency
Sample Size174
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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