A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608392



Internal ID20981463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112693301..112703100hg38UCSC Ensembl
chr7:112333356..112343155hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7087n223
Supporting Variantsnssv18226841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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