A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471263



Internal ID21128816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64272114..64274616hg38UCSC Ensembl
chr11:64039586..64042088hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382503
hg192503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178483
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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