A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584916



Internal ID21776959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73999096..73999096hg38UCSC Ensembl
chr11:73710141..73710141hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584916
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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