A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926472



Internal ID22701699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67335265..67338380hg38UCSC Ensembl
chr11:67102736..67105851hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383116
hg193116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364799
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926472
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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