A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187260



Internal ID20754300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6551671..6552252hg38UCSC Ensembl
chr11:6572901..6573482hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445773
Supporting Variants
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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