A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460211



Internal ID21117764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56226701..56228500hg38UCSC Ensembl
chr12:56620485..56622284hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001836
Samples
Known GenesNABP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460211
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