A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558874



Internal ID20931945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20396157..20397526hg38UCSC Ensembl
chr7:20435780..20437149hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273879
Samples
Known GenesITGB8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558874
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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