A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265683



Internal ID20474901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44139050..44139383hg38UCSC Ensembl
chr1:44604722..44605055hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265683
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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