A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921793



Internal ID22697017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78056678..78056976hg38UCSC Ensembl
chr11:77767724..77768022hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366800
Samples
Known GenesNDUFC2-KCTD14, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921793
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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