A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744085



Internal ID20520080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104974757..104975093hg38UCSC Ensembl
chr7:104615204..104615540hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744085
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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