A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734625



Internal ID20510563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75365199..75373699hg38UCSC Ensembl
chr11:75076243..75084743hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg388501
hg198501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734625
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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