A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435134



Internal ID21092687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21697798..21732311hg38UCSC Ensembl
chr8:21555310..21589823hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3834514
hg1934514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218473
Samples
Known GenesGFRA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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