A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454616



Internal ID21112169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31392001..31395000hg38UCSC Ensembl
chr10:31680930..31683929hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979183
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454616
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