A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443600



Internal ID21101153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100108670..100115421hg38UCSC Ensembl
chr10:101868427..101875178hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg386752
hg196752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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