A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907703



Internal ID22682913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126665228..126665538hg38UCSC Ensembl
chr9:129427507..129427817hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439592
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907703
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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