A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326209



Internal ID20859343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69450468..69470595hg38UCSC Ensembl
chr1:69916151..69936278hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3820128
hg1920128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326209
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