A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578046



Internal ID21526508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29268490..29268541hg38UCSC Ensembl
chr7:29308106..29308157hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141391
SamplesNA19239
Known GenesCHN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578046
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