A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409681



Internal ID21067234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6647143..6663439hg38UCSC Ensembl
chr6:6647376..6663672hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3816297
hg1916297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144272
Samples
Known GenesLY86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409681
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