A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357206



Internal ID21014759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87202584..87227054hg38UCSC Ensembl
chr3:87251734..87276204hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg3824471
hg1924471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210165
Samples
Known GenesMIR4795
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357206
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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