A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556670



Internal ID20929741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151454944..151455402hg38UCSC Ensembl
chr3:151172732..151173190hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263221
Samples
Known GenesIGSF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556670
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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