A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748403



Internal ID20524428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107888700..107888818hg38UCSC Ensembl
chr7:107529145..107529263hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748403
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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