A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330720



Internal ID20863878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151646388..151654516hg38UCSC Ensembl
chr1:151618864..151626992hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388129
hg198129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051346
Samples
Known GenesSNX27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330720
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