A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922243



Internal ID22697468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14007362..14007420hg38UCSC Ensembl
chr11:14028909..14028967hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359903
Samples
Known GenesSPON1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922243
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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