A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614871



Internal ID20987942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131961414..131961650hg38UCSC Ensembl
chr6:132282554..132282790hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614871
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