A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474856



Internal ID21132409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46355350..46355988hg38UCSC Ensembl
chr11:46376900..46377538hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193904, nssv17991764
Samples
Known GenesDGKZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474856
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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