A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399089



Internal ID21056642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87735801..87736200hg38UCSC Ensembl
chr6:88445519..88445918hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399089
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