A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362402



Internal ID22588071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128186729..128186729hg38UCSC Ensembl
chr11:128056624..128056624hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969379
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362402
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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