A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103075



Internal ID21465710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9277706..9277817hg38UCSC Ensembl
chr18:9277704..9277815hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587596
Supporting Variants
SamplesHG03065
Known GenesANKRD12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103075
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