A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073086



Internal ID21456477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473080hg38UCSC Ensembl
chr11:126342975..126342975hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648830
Supporting Variants
SamplesHG02492
Known GenesKIRREL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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