A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469612



Internal ID21127165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19943401..19952000hg38UCSC Ensembl
chr12:20096335..20104934hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469612
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