A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908348



Internal ID22683558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143047..62143154hg38UCSC Ensembl
chr11:61910519..61910626hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360577
Samples
Known GenesINCENP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908348
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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