A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130534



Internal ID21447956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304411..187304411hg38UCSC Ensembl
chr4:188225565..188225565hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626017
Supporting Variants
SamplesHG00732
Known GenesLOC339975
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130534
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