A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191406



Internal ID20758446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12473658..12555523hg38UCSC Ensembl
chr11:12495205..12577070hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3881866
hg1981866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455429
Supporting Variants
Samples
Known GenesPARVA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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