A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460371



Internal ID21117924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77897507..77901754hg38UCSC Ensembl
chr11:77608553..77612800hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185906
Samples
Known GenesINTS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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