A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060778



Internal ID21401540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150744433..150744433hg38UCSC Ensembl
chr1:150716909..150716909hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614755
Supporting Variants
SamplesHG00096
Known GenesCTSS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060778
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