A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497932



Internal ID274946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3266000..3594000hg38UCSC Ensembl
chr11:3287230..3615230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38328001
hg19328001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042154
Samples
Known GenesLOC650368, OR7E12P, ZNF195
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497932
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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