A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918772



Internal ID22693994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127687885..127693784hg38UCSC Ensembl
chr11:127557780..127563679hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918772
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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