A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926252



Internal ID22701479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19514495..19515817hg38UCSC Ensembl
chr11:19536042..19537364hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363267
Samples
Known GenesNAV2, NAV2-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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