A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705107



Internal ID21377383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44708225..44712081hg38UCSC Ensembl
chr11:44729775..44733631hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383857
hg193857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389814
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705107
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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