A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439051



Internal ID21096604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7934407..7940338hg38UCSC Ensembl
chr11:7955954..7961885hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385932
hg195932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994226
Samples
Known GenesOR10A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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