A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510149



Internal ID286777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93162431..93205597hg38UCSC Ensembl
chr11:92895597..92938763hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3843167
hg1943167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052035
Samples
Known GenesSLC36A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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