A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427887



Internal ID21085440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142747715..142769260hg38UCSC Ensembl
chr7:142455566..142475461hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3821546
hg1919896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7151n223
Supporting Variantsnssv18226950
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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