A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402199



Internal ID21059752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56189604..56194009hg38UCSC Ensembl
chr5:55485431..55489836hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg384406
hg194406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131790
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402199
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