A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411197



Internal ID21068750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142619679..142661849hg38UCSC Ensembl
chr5:141999244..142041414hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3842171
hg1942171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213224
Samples
Known GenesFGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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