A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060563



Internal ID20627603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25991609..26009134hg38UCSC Ensembl
chr1:26318100..26335625hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817526
hg1917526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322359
Supporting Variants
Samples
Known GenesPAFAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer