A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618288



Internal ID20991359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66656185..66683899hg38UCSC Ensembl
chr7:66121172..66148886hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3827715
hg1927715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225581
Samples
Known GenesRABGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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