A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559482



Internal ID20932553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20758405..20758699hg38UCSC Ensembl
chr7:20798028..20798322hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559482
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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