A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512037



Internal ID288604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3817475..3817562hg38UCSC Ensembl
chr11:3838705..3838792hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040635
Samples
Known GenesPGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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