A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473603



Internal ID21131156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10192849..10196110hg38UCSC Ensembl
chr12:10345448..10348709hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg383262
hg193262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473603
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