A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563784



Internal ID20936855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50152125..50152940hg38UCSC Ensembl
chr7:50191721..50192536hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274556
Samples
Known GenesC7orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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