A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583181



Internal ID21531702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6879814..6879876hg38UCSC Ensembl
chr4:6881541..6881603hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121473
SamplesHG00731
Known GenesKIAA0232
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583181
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