A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406918



Internal ID21064471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38202747..38208423hg38UCSC Ensembl
chr6:38170523..38176199hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385677
hg195677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141853
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406918
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