A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465975



Internal ID21123528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64785477..64802604hg38UCSC Ensembl
chr11:64552949..64570076hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3817128
hg1917128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196795
Samples
Known GenesMAP4K2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465975
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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