A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061373



Internal ID20628413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44077029..44080490hg38UCSC Ensembl
chr1:44542701..44546162hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg383462
hg193462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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