A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512757



Internal ID289304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32595013..32595965hg38UCSC Ensembl
chr11:32616559..32617511hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045608
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512757
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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