A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457846



Internal ID21115399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56312157..56469534hg38UCSC Ensembl
chr11:56079633..56237010hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38157378
hg19157378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993047
Samples
Known GenesOR5M3, OR5M9, OR5R1, OR8J1, OR8K1, OR8K3, OR8U1, OR8U8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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