A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617003



Internal ID20990074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95384062..95387983hg38UCSC Ensembl
chr7:95013374..95017295hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383922
hg193922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231682
Samples
Known GenesPON3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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