A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991767



Internal ID20558807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4638733..4650443hg38UCSC Ensembl
chr11:4659963..4671673hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811711
hg1911711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448771
Supporting Variants
Samples
Known GenesOR51D1, OR51E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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