A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747085



Internal ID20523101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64171765..64171992hg38UCSC Ensembl
chr11:63939237..63939464hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747085
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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