A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742575



Internal ID20518559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94176827..94176884hg38UCSC Ensembl
chr7:93806139..93806196hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742575
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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