A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199739



Internal ID20766779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114806389..114940228hg38UCSC Ensembl
chr1:115349010..115482849hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38133840
hg19133840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331836
Supporting Variants
Samples
Known GenesSYCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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