A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507314



Internal ID284038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61930562..61930676hg38UCSC Ensembl
chr11:61698034..61698148hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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