A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577341



Internal ID21525792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145366128..145366290hg38UCSC Ensembl
chr7:145063221..145063383hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154399
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577341
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