A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616183



Internal ID20989254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106111601..106113500hg38UCSC Ensembl
chr7:105752047..105753946hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7045n223
Supporting Variantsnssv18232522
Samples
Known GenesSYPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616183
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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