A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203562



Internal ID20770602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3004990..3396785hg38UCSC Ensembl
chr1:2921554..3313349hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38391796
hg19391796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317279
Supporting Variants
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203562
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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