A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398274



Internal ID21055827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131754749..131783479hg38UCSC Ensembl
chr5:131090442..131119172hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3828731
hg1928731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125133
Samples
Known GenesFNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398274
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