A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430399



Internal ID21087952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141592907..141594885hg38UCSC Ensembl
chr7:141292707..141294685hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381979
hg191979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217879
Samples
Known GenesAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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