A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555647



Internal ID20927689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158570023..158578008hg38UCSC Ensembl
chr3:158287812..158295797hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg387986
hg197986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259804
Samples
Known GenesLOC100996447, MLF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555647
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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