A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558035



Internal ID20931106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15667015..15668476hg38UCSC Ensembl
chr7:15706640..15708101hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381462
hg191462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6600n223
Supporting Variantsnssv18273785
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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