A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556602



Internal ID20929673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172688136..172689364hg38UCSC Ensembl
chr3:172405926..172407154hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259875
Samples
Known GenesNCEH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556602
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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