A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508291



Internal ID284986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35048998..35219698hg38UCSC Ensembl
chr11:35070545..35241245hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38170701
hg19170701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044188
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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