A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071807



Internal ID21410112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918724..70918878hg38UCSC Ensembl
chr10:72678481..72678635hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598747
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071807
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