A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420653



Internal ID21078206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135708984..135713654hg38UCSC Ensembl
chr7:135393732..135398402hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384671
hg194671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235109
Samples
Known GenesSLC13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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