A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423127



Internal ID21080680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19111196..19130183hg38UCSC Ensembl
chr9:19111194..19130181hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3818988
hg1918988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175537
Samples
Known GenesPLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423127
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