A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331836



Internal ID20865003
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 StatusM
Merged Variants
Supporting Variantsnssv18199739
Samples
Known GenesSYCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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