A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735763



Internal ID20511706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131633582..131633689hg38UCSC Ensembl
chr11:131503476..131503583hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289110
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735763
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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