A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501432



Internal ID278330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29788105..29798260hg38UCSC Ensembl
chr11:29809652..29819807hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3810156
hg1910156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501432
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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