A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437358



Internal ID21094911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7770730..7923864hg38UCSC Ensembl
chr11:7792277..7945411hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38153135
hg19153135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994156
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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