A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180673



Internal ID20747713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47972248..48741648hg38UCSC Ensembl
chr11:47993800..48763200hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38769401
hg19769401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459403
Supporting Variants
Samples
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180673
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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