A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566268



Internal ID20939339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23520265..23520380hg38UCSC Ensembl
chr7:23559884..23559999hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272715
Samples
Known GenesTRA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566268
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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