A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412748



Internal ID21070301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37690685..37693709hg38UCSC Ensembl
chr6:37658461..37661485hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg383025
hg193025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141815
Samples
Known GenesMDGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412748
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