A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328270



Internal ID20861416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155870997..155872385hg38UCSC Ensembl
chr1:155840788..155842176hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052101
Samples
Known GenesSYT11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328270
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