A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562574



Internal ID20935645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20178610..20180367hg38UCSC Ensembl
chr7:20218233..20219990hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273878
Samples
Known GenesMACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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