A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067185



Internal ID21454313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98232895..98240422hg38UCSC Ensembl
chr1:98698451..98705978hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg387528
hg197528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576514
Supporting Variants
SamplesHG02011
Known GenesLOC729987
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067185
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