A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365999



Internal ID22591668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59319012..59385198hg38UCSC Ensembl
chr11:59086485..59152671hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3866187
hg1966187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916680
Supporting Variants
Samples
Known GenesOR5AN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365999
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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