A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278625



Internal ID20487843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57030996..57031150hg38UCSC Ensembl
chr5:56326823..56326977hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278625
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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