A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221620



Internal ID20788660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68353014..68829975hg38UCSC Ensembl
chr7:67818001..68294962hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38476962
hg19476962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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