A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069479



Internal ID21466579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17828147..17832657hg38UCSC Ensembl
chr10:17870146..17874656hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587586
Supporting Variants
SamplesHG03065
Known GenesMRC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069479
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