A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486376



Internal ID21143929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119251510..119334251hg38UCSC Ensembl
chr12:119689315..119772056hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3882742
hg1982742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997379
Samples
Known GenesLINC00934
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486376
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