A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070197



Internal ID21436284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38087571..38087571hg38UCSC Ensembl
chr10:38376499..38376499hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628756
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070197
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