A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225581



Internal ID20792621
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 StatusS
Merged Variantsnsv6618288
Supporting Variants
Samples
Known GenesRABGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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