A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492803



Internal ID21150356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85124001..85129200hg38UCSC Ensembl
chr13:85698136..85703335hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492803
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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