A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265293



Internal ID20474511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156762627..156762752hg38UCSC Ensembl
chr1:156732419..156732544hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732434
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265293
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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