A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613286



Internal ID20986357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90556333..90592094hg38UCSC Ensembl
chr7:90185647..90221408hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835762
hg1935762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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