A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177501



Internal ID20744541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15612302..15612781hg38UCSC Ensembl
chr11:15633848..15634327hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177501
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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