A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475173



Internal ID21132726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69006766..69007358hg38UCSC Ensembl
chr11:68774234..68774826hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195178
Samples
Known GenesMRGPRF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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