A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290760



Internal ID20499978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107053164..107053319hg38UCSC Ensembl
chr4:107974321..107974476hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290760
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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