A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445773



Internal ID21103326
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 StatusM
Merged Variants
Supporting Variantsnssv18187260
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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