A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563597



Internal ID20936668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129842671..129843309hg38UCSC Ensembl
chr7:129482511..129483149hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271707
Samples
Known GenesUBE2H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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