A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397128



Internal ID21054681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64996186..65171101hg38UCSC Ensembl
chr6:65706079..65880994hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38174916
hg19174916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145664
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397128
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