A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061502



Internal ID20628542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53353963..53358509hg38UCSC Ensembl
chr1:53819635..53824181hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384547
hg194547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061502
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