A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268153



Internal ID20477371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219411137..219411256hg38UCSC Ensembl
chr1:219584479..219584598hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268153
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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