A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483064



Internal ID21140617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85171180..85257903hg38UCSC Ensembl
chr13:85745315..85832038hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3886724
hg1986724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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