A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742887



Internal ID20518872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146096082..146096160hg38UCSC Ensembl
chr7:145793175..145793253hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742887
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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