A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569382



Internal ID20942453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157162521..157163076hg38UCSC Ensembl
chr7:156955215..156955770hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273797
Samples
Known GenesUBE3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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