A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475397



Internal ID21132950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56149374..56499735hg38UCSC Ensembl
chr11:55916850..56267211hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38350362
hg19350362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992404
Samples
Known GenesOR5J2, OR5M3, OR5M8, OR5M9, OR5R1, OR5T1, OR5T2, OR5T3, OR8H1, OR8J1, OR8K1, OR8K3, OR8K5, OR8U1, OR8U8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer