A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071127



Internal ID21408040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6206743..6206858hg38UCSC Ensembl
chr10:6248706..6248821hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601655
Supporting Variants
SamplesHG00512
Known GenesPFKFB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071127
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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