A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180188



Internal ID20747228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3021495..3021991hg38UCSC Ensembl
chr11:3042725..3043221hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443940
Supporting Variants
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180188
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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