A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184774



Internal ID20751814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56491102..56501100hg38UCSC Ensembl
chr11:56258578..56268576hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg389999
hg199999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473471
Supporting Variants
Samples
Known GenesOR5M8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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