A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705239



Internal ID21377515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118560175..118560462hg38UCSC Ensembl
chr11:118430890..118431177hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390042
Supporting Variants
Samples
Known GenesIFT46
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705239
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0574713


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