A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109607



Internal ID20676647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147646516..147648165hg38UCSC Ensembl
chr4:148567667..148569316hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379971
Supporting Variants
Samples
Known GenesPRMT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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