A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705258



Internal ID21377534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131505052..131505304hg38UCSC Ensembl
chr11:131374946..131375198hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390080
Supporting Variants
Samples
Known GenesNTM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705258
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0201149


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