A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583868



Internal ID21775911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101509526..101517909hg38UCSC Ensembl
chr10:103269283..103277666hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg388384
hg198384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004799
Supporting Variants
Samples
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583868
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