A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606708



Internal ID20979779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4628192..4636264hg38UCSC Ensembl
chr7:4667823..4675895hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg388073
hg198073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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