A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925282



Internal ID22700509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9623316..10133753hg38UCSC Ensembl
chr11:9644863..10155300hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38510438
hg19510438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv226n209
Supporting Variantsnssv17361245
Samples
Known GenesLOC440028, SBF2, SBF2-AS1, SWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925282
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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