A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150710



Internal ID21480853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166898838..166898838hg38UCSC Ensembl
chr6:167312326..167312326hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639957
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150710
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