A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421876



Internal ID21079429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142749801..142760200hg38UCSC Ensembl
chr7:142457652..142468049hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810400
hg1910398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7152n223
Supporting Variantsnssv18229789
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421876
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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