A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112112



Internal ID20679152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148994701..149036000hg38UCSC Ensembl
chr4:149915853..149957152hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3841300
hg1941300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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