A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074375



Internal ID21438103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055116..36055116hg38UCSC Ensembl
chr11:36076666..36076666hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645648
Supporting Variants
SamplesHG00731
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074375
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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