A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457830



Internal ID21115383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25544003..25544420hg38UCSC Ensembl
chr12:25696937..25697354hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999844
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457830
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