A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144636



Internal ID20711676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8221941..8230219hg38UCSC Ensembl
chr6:8222174..8230452hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg388279
hg198279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398964
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer