A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735548



Internal ID20511491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117848076..117848132hg38UCSC Ensembl
chr10:119607587..119607643hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735548
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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