A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064035



Internal ID21452118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244486372..244486372hg38UCSC Ensembl
chr1:244649674..244649674hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616101
Supporting Variants
SamplesHG01596
Known GenesC1orf101
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064035
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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