A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202075



Internal ID20769116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5667631..5668216hg38UCSC Ensembl
chr1:5727691..5728276hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202075
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00204


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