A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292810



Internal ID20502028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40982037..40985438hg38UCSC Ensembl
chr5:40982139..40985540hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg383402
hg193402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740742
Supporting Variants
Samples
Known GenesC7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292810
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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