A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566982



Internal ID20940053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146032059..146033474hg38UCSC Ensembl
chr7:145729152..145730567hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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