A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432160



Internal ID21089713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142747501..142757700hg38UCSC Ensembl
chr7:142455352..142465547hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810200
hg1910196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7152n223
Supporting Variantsnssv18234882
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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