A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099349



Internal ID21410007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31597981..31597981hg38UCSC Ensembl
chr17:29925000..29925000hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654097
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099349
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