A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296620



Internal ID20505838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52662394..52662504hg38UCSC Ensembl
chr1:53128066..53128176hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296620
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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