A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582896



Internal ID21774939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3809005..3809111hg38UCSC Ensembl
chr10:3851197..3851303hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582896
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer