A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427769



Internal ID21085322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142749239..142760162hg38UCSC Ensembl
chr7:142457090..142468009hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810924
hg1910920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7152n223
Supporting Variantsnssv18218558
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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