A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456880



Internal ID22514760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240716407..240717933hg38UCSC Ensembl
chr1:240879707..240881233hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456880
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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