A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199245



Internal ID20766285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10961847..10970470hg38UCSC Ensembl
chr1:11021904..11030527hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388624
hg198624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317869
Supporting Variants
Samples
Known GenesC1orf127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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