A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062811



Internal ID21469573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222476200..222476609hg38UCSC Ensembl
chr1:222649542..222649951hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582466
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062811
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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