A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266584



Internal ID20475802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26868245..26868304hg38UCSC Ensembl
chr1:27194736..27194795hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266584
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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