A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456888



Internal ID21114441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46606126..46618934hg38UCSC Ensembl
chr11:46627676..46640484hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3812809
hg1912809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188904
Samples
Known GenesATG13, HARBI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456888
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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