A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203769



Internal ID20770809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15030864..15031362hg38UCSC Ensembl
chr21:16403185..16403683hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543779
Supporting Variants
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01183


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