A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608830



Internal ID20981901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159349644..159360335hg38UCSC Ensembl
chr6:159770676..159781367hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810692
hg1910692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608830
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