A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558349



Internal ID20931420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74384010..74384474hg38UCSC Ensembl
chr7:73798340..73798804hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276522
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558349
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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