A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063399



Internal ID21454903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221151793..221153006hg38UCSC Ensembl
chr1:221325135..221326348hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573920
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063399
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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