A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060155



Internal ID21432032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119016148..119016466hg38UCSC Ensembl
chr1:119558771..119559089hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583463
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060155
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