A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368796



Internal ID21026349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6707010..7549793hg38UCSC Ensembl
chr3:6748697..7591480hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38842784
hg19842784
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212995
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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