A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261787



Internal ID20471005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6000946..6001120hg38UCSC Ensembl
chr10:6042909..6043083hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741037
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261787
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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