A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633174



Internal ID21581479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304398..187304398hg38UCSC Ensembl
chr4:188225552..188225552hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130518
SamplesHG02011
Known GenesLOC339975
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633174
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