A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199738



Internal ID20766778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114776701..114809400hg38UCSC Ensembl
chr1:115319322..115352021hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3832700
hg1932700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317563
Supporting Variants
Samples
Known GenesSIKE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199738
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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