A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508955



Internal ID285628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35967041..35968543hg38UCSC Ensembl
chr11:35988591..35990093hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044260
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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