A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412817



Internal ID21070370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88160684..88161696hg38UCSC Ensembl
chr5:87456501..87457513hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412817
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