A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704859



Internal ID21377135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49069971..49070287hg38UCSC Ensembl
chr10:50278016..50278332hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389361
Supporting Variants
Samples
Known GenesVSTM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704859
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.195402


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