A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736936



Internal ID20512890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430914..28431125hg38UCSC Ensembl
chr11:28452461..28452672hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736936
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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