A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458800



Internal ID21116353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104009347..104658697hg38UCSC Ensembl
chr11:103880075..104529425hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38649351
hg19649351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189143
Samples
Known GenesDDI1, PDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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