A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191446



Internal ID20758486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130563109..131175248hg38UCSC Ensembl
chr11:130433004..131045143hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38612140
hg19612140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462284
Supporting Variants
Samples
Known GenesC11orf44, MIR8052, SNX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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