A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455616



Internal ID21113169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69174488..69178295hg38UCSC Ensembl
chr12:69568268..69572075hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383808
hg193808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455616
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