A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224999



Internal ID20792039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142746897..142768261hg38UCSC Ensembl
chr7:142454748..142475461hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3821365
hg1920714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422199
Supporting Variants
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224999
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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