A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389448



Internal ID21047001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38088915..38089461hg38UCSC Ensembl
chr4:38090536..38091082hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115995
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389448
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