A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603340



Internal ID20976411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125236564..125259112hg38UCSC Ensembl
chr7:124876618..124899166hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3822549
hg1922549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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