A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607240



Internal ID20980311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11942981..12021852hg38UCSC Ensembl
chr7:11982607..12061478hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3878872
hg1978872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607240
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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