A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121435



Internal ID21419967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43343668..43343668hg38UCSC Ensembl
chr4:43345685..43345685hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623892
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121435
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