A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618128



Internal ID20991199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98404041..98404542hg38UCSC Ensembl
chr6:98851917..98852418hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618128
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