A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483284



Internal ID21140837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109721301..109819300hg38UCSC Ensembl
chr13:110373648..110471647hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3898000
hg1998000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1994n223
Supporting Variantsnssv18183889
Samples
Known GenesIRS2, LINC00676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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