A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373092



Internal ID21030645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129309491..129318505hg38UCSC Ensembl
chr3:129028334..129037348hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg389015
hg199015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093214
Samples
Known GenesH1FX, H1FX-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373092
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