A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409218



Internal ID21066771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77750901..77812400hg38UCSC Ensembl
chr5:77046725..77108224hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3861500
hg1961500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214143
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409218
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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