A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626407



Internal ID21574712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93140180..93140180hg38UCSC Ensembl
chr7:92769493..92769493hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152823
SamplesNA12878
Known GenesSAMD9L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626407
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