A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557693



Internal ID20930764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23367275..23367718hg38UCSC Ensembl
chr7:23406894..23407337hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6619n223
Supporting Variantsnssv18272694
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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