A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499096



Internal ID276075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31531002..31578908hg38UCSC Ensembl
chr11:31552549..31600455hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3847907
hg1947907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044604
Samples
Known GenesELP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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