A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044721



Internal ID97560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19400287..19400291hg38UCSC Ensembl
chr11:19421834..19421838hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535072
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044721
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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