A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580470



Internal ID21772513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65540721..65540721hg38UCSC Ensembl
chr11:65308192..65308192hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084331
Supporting Variants
Samples
Known GenesLTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580470
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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