A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462932



Internal ID21120485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126091485..126097067hg38UCSC Ensembl
chr11:125961380..125966962hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385583
hg195583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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