A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115984



Internal ID20683024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37856189..37895442hg38UCSC Ensembl
chr4:37857810..37897063hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3839254
hg1939254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389560
Supporting Variants
Samples
Known GenesPGM2, TBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115984
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