A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177542



Internal ID20744582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11557300..11570843hg38UCSC Ensembl
chr11:11578847..11592390hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813544
hg1913544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436176
Supporting Variants
Samples
Known GenesGALNT18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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