A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571363



Internal ID20944434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185697504..185698020hg38UCSC Ensembl
chr3:185415292..185415808hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261232
Samples
Known GenesIGF2BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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