A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439014



Internal ID21096567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15063141..15069766hg38UCSC Ensembl
chr11:15084687..15091312hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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