A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562343



Internal ID20935414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23355307..23355744hg38UCSC Ensembl
chr7:23394926..23395363hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272691
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562343
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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