A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704970



Internal ID21377246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114328109..114328556hg38UCSC Ensembl
chr10:116087868..116088315hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389561
Supporting Variants
Samples
Known GenesAFAP1L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704970
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0201149


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