A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334522



Internal ID20867709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167079688..167085149hg38UCSC Ensembl
chr1:167048925..167054386hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg385462
hg195462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053541
Samples
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334522
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