A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352179



Internal ID22577848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10333508..10333508hg38UCSC Ensembl
chr11:10355055..10355055hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977242
Supporting Variants
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352179
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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