A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368515



Internal ID21026068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7148425..7212805hg38UCSC Ensembl
chr3:7190112..7254492hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3864381
hg1964381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208689
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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