A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981005



Internal ID21890348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118634660..118634927hg38UCSC Ensembl
chr1:119177283..119177550hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981005
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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