A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747265



Internal ID20523282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37940506..37940831hg38UCSC Ensembl
chr11:37962056..37962381hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747265
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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