A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907786



Internal ID22682996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63854693..63855198hg38UCSC Ensembl
chr11:63622165..63622670hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364515
Samples
Known GenesMARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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