A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059798



Internal ID21439059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117029204..117029204hg38UCSC Ensembl
chr1:117571826..117571826hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613004
Supporting Variants
SamplesHG00732
Known GenesCD101
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer