A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502528



Internal ID279389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83700928..83720126hg38UCSC Ensembl
chr11:83411971..83431169hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3819199
hg1919199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048875
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502528
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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