A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062813



Internal ID21401102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222480383..222483522hg38UCSC Ensembl
chr1:222653725..222656864hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383140
hg193140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566309
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062813
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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