A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356200



Internal ID21013753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71288537..71338702hg38UCSC Ensembl
chr3:71337688..71387853hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3850166
hg1950166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208687
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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