A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155242



Internal ID21452763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144824472..144824472hg38UCSC Ensembl
chr6:145145608..145145608hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632909
Supporting Variants
SamplesHG01596
Known GenesUTRN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155242
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