A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226836



Internal ID20793876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77385293..77498748hg38UCSC Ensembl
chr7:77014610..77128065hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38113456
hg19113456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608583
Supporting Variants
Samples
Known GenesGSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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