A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151055



Internal ID21460769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103452475..103456140hg38UCSC Ensembl
chr7:103092922..103096587hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583563
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151055
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