A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526233



Internal ID20899594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28377231..29769380hg38UCSC Ensembl
chr19:28868138..30260287hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381392150
hg191392150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046097
Samples
Known GenesC19orf12, LINC00906, LOC100505835, LOC284395, PLEKHF1, POP4, UQCRFS1, VSTM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526233
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