A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087506



Internal ID21433954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10107404..10107404hg38UCSC Ensembl
chr17:10010721..10010721hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655735
Supporting Variants
SamplesHG00731
Known GenesGAS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087506
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