A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500902



Internal ID277823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6409644..6409837hg38UCSC Ensembl
chr11:6430874..6431067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041696
Samples
Known GenesAPBB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500902
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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