A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915874



Internal ID22691092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5712171..5716077hg38UCSC Ensembl
chr11:5733401..5737307hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383907
hg193907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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