A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203668



Internal ID20770708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63105227..63388192hg38UCSC Ensembl
chr1:63570898..63853863hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38282966
hg19282966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331505
Supporting Variants
Samples
Known GenesALG6, FOXD3, LINC00466, MIR6068
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203668
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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