A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138033



Internal ID21418106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169079819..169079819hg38UCSC Ensembl
chr5:168506824..168506824hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626945
Supporting Variants
SamplesHG00731
Known GenesSLIT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138033
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