A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295203



Internal ID20504421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38390732..38390856hg38UCSC Ensembl
chr8:38248250..38248374hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744077
Supporting Variants
Samples
Known GenesLETM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295203
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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