A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560817



Internal ID20933888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97145478..97146733hg38UCSC Ensembl
chr7:96774790..96776045hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275766
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560817
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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