A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502535



Internal ID279396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118139470..118144865hg38UCSC Ensembl
chr11:118010185..118015580hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385396
hg195396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688438
Samples
Known GenesSCN4B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502535
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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