A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331669



Internal ID20864834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2084685..2088351hg38UCSC Ensembl
chr1:2016124..2019790hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057191
Samples
Known GenesPRKCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331669
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