A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475682



Internal ID21133235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96676701..96771200hg38UCSC Ensembl
chr13:97328955..97423454hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3894500
hg1994500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183386
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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