A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199892



Internal ID20766932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207364001..207384800hg38UCSC Ensembl
chr1:207537346..207558145hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3820800
hg1920800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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