A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552450



Internal ID20925578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66977254..66977928hg38UCSC Ensembl
chr1:67442937..67443611hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251256
Samples
Known GenesMIER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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