A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131165



Internal ID21448279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1940891..1940946hg38UCSC Ensembl
chr4:1942618..1942673hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570511
Supporting Variants
SamplesHG00864
Known GenesWHSC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131165
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer