A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481061



Internal ID22538965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56140079..56141478hg38UCSC Ensembl
chr1:56605751..56607150hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481061
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