A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203479



Internal ID20770519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26564101..26565700hg38UCSC Ensembl
chr1:26890592..26892191hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321306
Supporting Variants
Samples
Known GenesRPS6KA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01839


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