A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109604



Internal ID20676644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147603539..147659052hg38UCSC Ensembl
chr4:148524690..148580203hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3855514
hg1955514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386640
Supporting Variants
Samples
Known GenesPRMT10, TMEM184C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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