A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447693



Internal ID21105246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11753867..11760860hg38UCSC Ensembl
chr10:11795866..11802859hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386994
hg196994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978317
Samples
Known GenesECHDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447693
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