A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566272



Internal ID20939343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70019070..70025619hg38UCSC Ensembl
chr7:69484056..69490605hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg386550
hg196550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275070
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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