A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705700



Internal ID21377976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21119567..21119707hg38UCSC Ensembl
chr14:21587726..21587866hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390908
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705700
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0747126


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