A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532131



Internal ID20905492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23972376..24100606hg38UCSC Ensembl
chr19:24155178..24283408hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38128231
hg19128231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046003
Samples
Known GenesZNF254
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532131
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