A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469977



Internal ID21127530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62103240..62127744hg38UCSC Ensembl
chr11:61870712..61895216hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3824505
hg1924505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184461
Samples
Known GenesINCENP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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