A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065043



Internal ID20632083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84269939..84275372hg38UCSC Ensembl
chr1:84735622..84741055hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385434
hg195434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065043
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