A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522251



Internal ID20895612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20386680..21525688hg38UCSC Ensembl
chr19:20497489..21708490hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381139009
hg191211002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045515
Samples
Known GenesLINC00664, MIR1270-1, MIR1270-2, ZNF429, ZNF430, ZNF431, ZNF493, ZNF626, ZNF708, ZNF714, ZNF737, ZNF738, ZNF826P, ZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522251
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