A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319772



Internal ID20852869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203942095..204097521hg38UCSC Ensembl
chr1:203911223..204066649hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38155427
hg19155427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201847
Samples
Known GenesLINC00303, SOX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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